| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs185110805 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9631201 | ACCTACAAGGCTCCA[C/T]GTGAATTTCTGTCCT | 146845 |
| rs185126865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9609074 | ATACCCCACACATGT[A/G]CTTTATGGCCTCTGC | 146845 |
| rs185134409 | snp | A/G | 1.64738e-05 | 0.00286995 | missense | CFAP52 | GRCh38.p7 | 17:9635444 | CAGACCCAGAAGCTG[A/G]AGGAGGCCCTGAAGG | 146845 |
| rs185169278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9601864 | CTCGTTTCTGATAAC[A/G]GAACAGATGGTTCTA | 146845 |
| rs185191733 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585396 | AGTGTTGGCCGGGCG[C/T]GGTGGCTCACACCTG | 146845 |
| rs185268329 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CFAP52 | GRCh38.p7 | 17:9592965 | AATTTTTCCACTTTT[C/G]ATGGTATCTGTTAAT | 146845 |
| rs185351268 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9636708 | AAAGAACATGAGATA[C/T]GCTTGATGGGAATGA | 146845 |
| rs185352302 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586280 | AGAAAAGTGATAGAG[C/T]GGGCTGGGCGCGGTG | 146845 |
| rs185358048 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CFAP52 | GRCh38.p7 | 17:9612741 | AGTACCTGACAAAAC[C/T]TTTCTGTTTTCTTAA | 146845 |
| rs185452810 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP52 | GRCh38.p7 | 17:9630667 | GATCTCCTGACCTCG[C/T]GATCCGCCCGCCTCG | 146845 |
| rs185488895 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9608530 | GATGTTATAAACTTA[A/T]CCAAGAAATAACCCC | 146845 |
| rs185494424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9639708 | GTGACATGATACTGG[C/T]GGGCGGGGGAAAGCT | 146845 |
| rs185607374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9588578 | TCTACCCACTCACCT[C/T]GGACTTCAGCATGGG | 146845 |
| rs185613643 | snp | A/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575126 | GGGATCAAAAGTTGC[A/T]TCTTTCATCATGCAG | 146845 |
| rs185624585 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9578331 | GAAGCCTCAGTAAAC[C/T]GGCCAGAGGTAGTCC | 146845 |
| rs185804338 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9623635 | AAGTTGTCATCTGTT[A/T]CCTTTCCCCTCTCTA | 146845 |
| rs185835955 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9634029 | CATCAATTATTAAAT[A/G]CACCCAGACGTTTTG | 146845 |
| rs185883706 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642350 | TAAATGCGGCCAGGC[A/G]TGGTGGCTCATGCCT | 146845 |
| rs185907275 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9640969 | CATTTTCTTTATGCA[G/T]TCTATCATTGATGGG | 146845 |
| rs185925159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598439 | GGGGATAGGAAAGTG[A/G]GGTATAGACATAGGG | 146845 |
| rs186044061 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | CFAP52 | GRCh38.p7 | 17:9622578 | AGAAGAAGAAGATGA[A/T]GATGATGATGAGTAG | 146845 |
| rs186062128 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9582477 | CTGGCTATCCATATC[A/C]TTTGCTCATTTTTCT | 146845 |
| rs186226984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9628568 | AGGTTTGAGCCACCG[C/T]GCCCAGCCTTTTCCT | 146845 |
| rs186311649 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9579310 | GAAGGCAGAATATTT[C/T]GGGTTACAGCAATAG | 146845 |
| rs186330428 | snp | G/T | 4.94336e-05 | 0.00497135 | synonymous-codon, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641774 | CAGAGAATTGGAAGG[G/T]TCCCTGTCTGGGTCG | 146845 |
| rs186357526 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9583549 | AATGGAAAATGCTAC[C/T]AGAAGGCATAAAAGG | 146845 |
| rs186386118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9604851 | GGAAAGATACTCTAT[A/G]TCTTATATCAGCCGG | 146845 |
| rs186484782 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9583763 | AAAATTCTGACCATA[A/G]GTGAGCAATAATGGA | 146845 |
| rs186533411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9627489 | AGCCCAGGCAACAGA[A/G]TGAGACTCCATCTCA | 146845 |
| rs186547446 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9602941 | GTGTGTTCATATAGG[A/T]TAGGAATTCTAATAT | 146845 |
| rs186551005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585642 | GCACCATTGCACCCC[A/G]GGCTGGGTGACAAGT | 146845 |
| rs186675771 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600436 | TTAGTACAGACAGGG[A/T]TTCATCATGTTGGCT | 146845 |
| rs186713483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9603410 | GAGACGGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 146845 |
| rs186802863 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9611400 | CACTCTGTCATCCAG[G/T]ATGGAGGGCAGGGAT | 146845 |
| rs186887709 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633883 | AGACGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 146845 |
| rs186937052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585979 | GGGTTCAAGGTGAAT[A/G]CAGTGAAAACGACTC | 146845 |
| rs186992143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9588200 | CACAGCCATGTTGCC[A/G]TAGCATGGGAAAGGC | 146845 |
| rs187015432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9627783 | TGGAGTGCAGTGGCA[C/T]GATCATAGCTCAATG | 146845 |
| rs187029357 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9613815 | TGAGCCACTGCACCC[A/G]GCCTCAGACCTCAGT | 146845 |
| rs187115332 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9638358 | GTGCTCTGTCTTTAG[A/G]AAAGGGCCCTTCCCA | 146845 |
| rs187264084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9577728 | CAAGATCATTGAGAA[A/G]CAATTGAGCAGCCTA | 146845 |
| rs187325231 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9613210 | GGCTTCATGGTGGTG[A/G]GTATTACGAGGGCTT | 146845 |
| rs187332485 | snp | C/T | 0.000511302 | 0.0159809 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9632976 | CAGGATCGGCGTCAC[C/T]GCCATCGCCACCACC | 146845 |
| rs187335384 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9610936 | CTGTGGGCTAGCAAC[A/G]GATATAAAGGAGCAA | 146845 |
| rs187343718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9590376 | ATCTGCTGGTGGGAG[A/G]TGGCCTTGGCAATTT | 146845 |
| rs187351706 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CFAP52 | GRCh38.p7 | 17:9579631 | GGAGTGCAGTGGTGC[A/G]ATCTCAGCTCACTGC | 146845 |
| rs187477811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9580204 | GGAATGTAGCTATGC[C/T]CATTTGTTTATGTAT | 146845 |
| rs187537797 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | CFAP52 | GRCh38.p7 | 17:9637583 | TATGCACATAAAAAT[A/C]AACTGAAATGCTGGT | 146845 |
| rs187542419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9613620 | CCTCCTCGATTCAAG[C/T]GATTCTCCTGCCTCA | 146845 |
| rs187546816 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9594410 | TGATCTGGGGGAACA[C/T]GTCTTTAGTCCTGGA | 146845 |
| rs187575858 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | CFAP52 | GRCh38.p7 | 17:9636970 | GAATCGCTTGAACCC[A/G]GGAGGCGGAGGTTGC | 146845 |
| rs187586104 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9601462 | TTCACCTCTTCAAAG[C/T]ATAGGGCCTATTGCT | 146845 |
| rs187597736 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9593473 | TTTGTTTTTTGTTTT[C/T]GAGACGCAGTCTCGC | 146845 |
| rs187603624 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9585246 | GAAATCAGAATCTGC[A/C]TTTTAACAGGATCCC | 146845 |
| rs187608770 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642645 | TAAGTAAAAAATAAA[A/T]AAATGCATGAAATGA | 146845 |
| rs187613441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9578103 | TCTCAAAAAATAAAT[A/G]AATAAATAAACAAAC | 146845 |
| rs187618909 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600722 | GGCGCCCGCCACCAC[A/G]CCCAGCTAATTTTTT | 146845 |
| rs187702285 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9626140 | CTCAGACCCTAAACT[A/G]AGAACAATCTACCAC | 146845 |
| rs187849695 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9594913 | TTTTTTTTTTTTTGA[C/G]AGTGTTTTGCTGTGT | 146845 |
| rs187863628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586974 | TTCATCAACCAGGTG[C/T]TCAGCCTAGTACCCA | 146845 |
| rs187885192 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CFAP52 | GRCh38.p7 | 17:9625181 | GCTGTCTTTAGCAGT[A/G]GAATCCTTAAAAAAA | 146845 |
| rs187903909 | snp | A/C | 0.00433982 | 0.0463797 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584377 | AGAGCACCTGGTGGG[A/C]ACTCAGAACTGAAAC | 146845 |
| rs187905793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9629843 | AATCCACCCGCCTCG[A/G]CCTCCCAAAGTGATG | 146845 |
| rs187946323 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9629258 | AGGCAGCGTGATATT[C/G]CACCTCTAAAGACTT | 146845 |
| rs187950422 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9605294 | ATAAAGTCAGGAAAA[G/T]ACTTTATAGGAAAAG | 146845 |
| rs188134133 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9580613 | AGGATCACCTGAGCC[C/T]GGGAGGTAGAGGCTG | 146845 |
| rs188380864 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585564 | TAATCCCAGCTACTC[A/G]GGAGGCTGAAGCAGG | 146845 |
| rs188392035 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9606496 | TGATCTCATTCGATC[G/T]TCATAAACGCCTAAT | 146845 |
| rs188448391 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | CFAP52 | GRCh38.p7 | 17:9640825 | ATTTTTGTATTTTTA[G/T]TACAGACAGGGTTTC | 146845 |
| rs188619696 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | CFAP52 | GRCh38.p7 | 17:9607352 | CTCTGCCTCAAAAAA[A/C]CAATAGTAATAACAA | 146845 |
| rs188627526 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CFAP52 | GRCh38.p7 | 17:9587916 | AAAAATACCATAAAA[A/G]TGGTTTTCAAAGTTG | 146845 |
| rs188638860 | snp | A/G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9632533 | CAGGAGAAAGATGGT[A/G/T]GTGCCTTGGATGAAG | 146845 |
| rs188653924 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CFAP52 | GRCh38.p7 | 17:9589606 | GGCATGGTGGCAGGC[A/G]CCTGTAATCCCATCT | 146845 |
| rs188668441 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CFAP52 | GRCh38.p7 | 17:9629387 | ACACATACTGCTTCA[C/T]ATCAATGAAAAGTTC | 146845 |
| rs188686176 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9587720 | AATGGAGTTTTTGTT[C/T]TATCTTATAAATTTA | 146845 |
| rs188696248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9592598 | TTCTAAAACATTTCT[C/T]ATAAGTAGAATCATA | 146845 |
| rs188709331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9579035 | GGGAACTCTGCTTTA[A/G]GGTGTTTTGGGGGTC | 146845 |
| rs188786345 | snp | A/G | 0.000148276 | 0.00860907 | missense | CFAP52 | GRCh38.p7 | 17:9635504 | GTGAAGAGGAACAAC[A/G]AGGAGTGTGTCACCG | 146845 |
| rs188788396 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9612551 | TAATTTTATGAATGC[A/C]TTTTCAATATTAATG | 146845 |
| rs188918885 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | CFAP52 | GRCh38.p7 | 17:9610007 | AGAGAGAGAGAGAGA[C/G]AGAGACAGAGACAGA | 146845 |
| rs188939658 | snp | C/G | 0.00398755 | 0.0445055 | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576894 | GGAGCCCTGGCCAGG[C/G]ACACGCACAGGAGGA | 146845 |
| rs188943097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9596914 | TAGAGACGGGGTTTT[C/T]ACCATGTTGGCCAGG | 146845 |
| rs188945553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9614542 | AAATAACATTTACTA[A/G]TTAGGAATTTTTGCT | 146845 |
| rs188949579 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9581684 | GTAGTTTTGGTTACT[C/T]ATATCTGAATACTAT | 146845 |
| rs188965360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9581241 | AGAATGGCGTGAACC[C/T]GGAAGTGCTGGTTGC | 146845 |
| rs189006381 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CFAP52 | GRCh38.p7 | 17:9622718 | GTATTGAAGTATAAC[A/G]TATATGCAAAATACA | 146845 |
| rs189019940 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9640198 | TGCACGTGCAGGTTT[A/G]CACTCCTGATTCCTG | 146845 |
| rs189031972 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CFAP52 | GRCh38.p7 | 17:9615629 | TTGAATTGTTTTTTT[G/T]TCTTTTAGGACATAA | 146845 |
| rs189240354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9596677 | TACCTTGAAAAAAAC[A/G]CATTTAAACTTACTC | 146845 |
| rs189259465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9602532 | AGTCTATCATTGATG[A/G]ACATTTGGGTTGGTT | 146845 |
| rs189287953 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9641249 | CAGAAGGGAAAGTTG[A/G]GAATAAGGGTGGTGT | 146845 |
| rs189298313 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598526 | CAGCATTTTGGGAGG[C/T]GGAGGTGGGTGAATC | 146845 |
| rs189374466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9627510 | CTCCATCTCAAAAAT[A/G]AATAAATAAATGAAT | 146845 |
| rs189389151 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, missense | CFAP52 | GRCh38.p7 | 17:9585807 | CAAATGCCATCCTGA[A/C]CAGGAGCATATGATT | 146845 |
| rs189493783 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9597671 | AGCTGGGCGTGGTGG[C/T]GGGCACCTGTAGTCC | 146845 |
| rs189529150 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632064 | AGGTATGAGCCACTG[C/T]GCCCAGCCTCCACTT | 146845 |
| rs189540750 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9627082 | TAATCTTTTGACACA[A/T]TGGTAATTTACATTG | 146845 |
| rs189543109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9609180 | GTGTTGAACATTCAC[A/G]GGGTACCAGGCATCA | 146845 |
| rs189616880 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CFAP52 | GRCh38.p7 | 17:9630296 | TTAAAATGTAAGTCA[A/G]GGCCAGGCGCGGTGG | 146845 |
| rs189620315 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CFAP52 | GRCh38.p7 | 17:9608001 | TCATTAATATTTAAA[A/T]TTTTTTTTATTGCCA | 146845 |
| rs189621637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9588140 | ATGTTTACATCCTGC[A/G]TGACTCAGCAAGTTT | 146845 |
| rs189749485 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | CFAP52 | GRCh38.p7 | 17:9626840 | AATGTGTGGAAGGGA[A/T]CCACTTATTTTTTGT | 146845 |
| rs189765133 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9622247 | TCAGAAACAATCTAT[A/G]TACAGAAAATATGGT | 146845 |
| rs189770835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585400 | TTGGCCGGGCGCGGT[A/G]GCTCACACCTGTAAT | 146845 |
| rs189771722 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9636752 | ACTTAATACATTAAA[A/G]AACACAAAGCACTGC | 146845 |
| rs189773762 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586339 | GAGGCCTAGACGGTC[A/G]GATCCCCTGAGGTCA | 146845 |
| rs189779203 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9582243 | CATTGTTTTCCAAAA[C/T]GATTAGACCGATTTA | 146845 |
| rs189804312 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9588318 | GAGAGAGCCAGAGCT[C/G]TCCATCTTTGCAGAT | 146845 |
| rs189850829 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9629059 | GCATATAGCGTGAAT[A/C]TTTCTCTCTAGTAGG | 146845 |
| rs190012629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9602111 | TGGTTTTTCTAATTC[C/T]TTTTAGGATAGGAAT | 146845 |
| rs190016078 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9588809 | TGGAGTTTCACTCTT[G/T]TTGCCCAGGCTGGAG | 146845 |
| rs190026261 | snp | C/G/T | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575472 | CCAGGGAAGCCTGCA[C/G/T]CAGCCAGCTAGCTCC | 146845 |
| rs190083959 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9574675 | GAGTAGCTGGGATTA[C/T]AGGCATGTACTACCA | 146845 |
| rs190096821 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9631147 | TAGGGCTCAAAAGTC[A/T]TTTACCCTCTAAGAG | 146845 |
| rs190102644 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CFAP52 | GRCh38.p7 | 17:9608903 | TATGTACACACGAAA[G/T]AAGTCACTACCAGAC | 146845 |
| rs190299710 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CFAP52 | GRCh38.p7 | 17:9634314 | AGCATCTGACTACTA[C/T]GTTTTCTGGTGTAGT | 146845 |
| rs190310727 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CFAP52 | GRCh38.p7 | 17:9630682 | TGATCCGCCCGCCTC[A/G]GTCTCCCAAAGTGCT | 146845 |
| rs190322559 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CFAP52 | GRCh38.p7 | 17:9591554 | CAGATCTCTATGTTG[C/T]TGCCCTTTGTTTTAT | 146845 |
| rs190327138 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CFAP52 | GRCh38.p7 | 17:9588268 | GATAATTGCCCTGTG[A/G]ACACTGTGCAGGTGC | 146845 |
| rs190452870 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9613653 | CTCCTGAGTAGCTAG[A/G]ATTACAGGCATGCAC | 146845 |
| rs190461240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9594468 | ATTTTGTACTCATTA[A/G]AAGTTCTCTTCACTG | 146845 |
| rs190466031 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9580302 | AGCCTAAAATATTTA[C/T]TCTCTGGACCTTTCT | 146845 |
| rs190532950 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638090 | ATGATATGGTACGTC[A/C]AAACCTGTGTACAAA | 146845 |
| rs190565524 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9611966 | TTAGGATTATTTTTC[A/C]GAAGTGGAATTAATA | 146845 |
| rs190581959 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9578344 | ACTGGCCAGAGGTAG[A/T]CCGTGGTGAGTGGTC | 146845 |
| rs190615282 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9589484 | ACGCCTGAAATCCCA[A/G]CACTTTGGGAGGCCG | 146845 |
| rs190689605 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9623114 | TGTTTTGCATATCTT[A/T]AAGCTCTGTTATTAG | 146845 |
| rs190700519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9599442 | ACACCTTTATCCTAG[A/G]AGCCCTTAAGAGATG | 146845 |
| rs190708787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9583603 | GTTTTTAAAATAGAG[A/G]TATTTTATATTATTA | 146845 |
| rs190781220 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642207 | TATTATTGCATGATG[C/T]GATGCCCTTCCCACC | 146845 |
| rs190842429 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9612790 | TAGTACAGACAGTCC[C/T]TGACTTATGATTTTT | 146845 |
| rs190864670 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9579493 | TTTAGATTTCAGATG[A/G]AAACAAATTAGAAAC | 146845 |
| rs190872515 | snp | C/T | 0.000207684 | 0.0101882 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575761 | TCCCCGAAGGTCCCT[C/T]CACGCACCGCCGCCC | 146845 |
| rs191090891 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600982 | GTCATTGGCGGCACT[A/G]TTCACAATAGCAAAG | 146845 |
| rs191100817 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584717 | ACCTCCGCCTCGTGG[G/T]TTCCAGTGATTCTCC | 146845 |
| rs191105516 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9593013 | GGAGAATTTATGGCT[A/C]TTATATGACTTCCTA | 146845 |
| rs191146003 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642481 | ACACAAAAATTAGCC[A/G]GGCGTGGTGGTGCAC | 146845 |
| rs191164063 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600498 | TCTGCCCACCTTGGC[A/C]TCTCAAAGTGCTGGG | 146845 |
| rs191186747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9582591 | GAAAATATCTTCTTG[C/T]TTGTGTTTTTCTCTT | 146845 |
| rs191301974 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633923 | CCTGACCTCGTGATC[C/T]GCCTGCCTCGGCCTC | 146845 |
| rs191399934 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9627931 | GCAGGGTCTCACTAT[A/G]TTGCCCAGGCTGGTC | 146845 |
| rs191401020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9624312 | TTATCTGTGTTTAGT[A/G]ATTTGAGATTTTCCT | 146845 |
| rs191415134 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584164 | TGGTCATTGTATTTT[A/C]TTTTATTTTTGCTGA | 146845 |
| rs191419669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586131 | TTCATTCCGTCAGAC[C/T]GGGAGTGAAGGACTC | 146845 |
| rs191527919 | snp | A/C/G/T | 0.00676609 | 0.0577691 | intron-variant | CFAP52 | GRCh38.p7 | 17:9629951 | CCTACCCCACCCTGC[A/C/G/T]CATGTCTTCTCCACA | 146845 |
| rs191534377 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CFAP52 | GRCh38.p7 | 17:9607572 | TCAGATAATACAGTC[A/G]CCAAACAATAAGAAG | 146845 |
| rs191543956 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9588000 | TACCTTCCAAGAGTC[C/T]GATTTGATTGGCCTG | 146845 |
| rs191640305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9577077 | GTTGTAACCCTTCTC[C/T]CACTAGGTCAGCCCT | 146845 |
| rs191664705 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9603537 | TCATGTTCATGGATA[A/G]GAAGACTCAGTATTG | 146845 |
| rs191730110 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9610276 | CCTTCTAATTTTTTA[A/C]CCCTTTGTTTTTAGT | 146845 |
| rs191742938 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9633476 | TCCCAAAGTGCTGGG[A/C]TTACAGGTATGAGCA | 146845 |
| rs191743015 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9611021 | AGGCCAGAGGTTTCT[A/G]ACAACTTGTCCAGAG | 146845 |
| rs191753721 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9590507 | CACTGCAGCGAAAGA[A/G]AAGAGTTCCAACATC | 146845 |
| rs191762681 | snp | C/G | | | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9577773 | ATGTCACTTGTTGAG[C/G]CAATGTAGAACCACA | 146845 |
| rs191941938 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9640444 | GTTGTTTCCCCACGT[G/T]TCCATCTCTTTTCAT | 146845 |
| rs191946802 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9615986 | AAATATAGTTTTTCG[C/G/T]GGGGAGGAGCCAAGA | 146845 |
| rs191946860 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9637020 | ACTGCACTCCAGCCT[A/G]GGCCACAGAGTGAGA | 146845 |
| rs191961060 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9593760 | CGCTCCCAGCCAACA[C/T]TCGAAACCATCCTGG | 146845 |
| rs192007953 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632754 | CTATGGTGACCAGCA[C/T]TCAGCTGAGCTGGTC | 146845 |
| rs192032155 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9589830 | TGCAAGCAGAAAAAG[A/C]CTTGTTTTATTTTAA | 146845 |
| rs192191941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9580071 | TTCCTATTATGGTAT[A/G]CAAAGAGTTCTTGTA | 146845 |
| rs192219406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9626291 | CTGGAGTGTAATGGC[A/G]TGATCTCAGCTCACT | 146845 |
| rs192223263 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9601705 | AGTTAGAGACTTTGA[A/T]ATTTATACCAAAATA | 146845 |
| rs192223299 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9625274 | GGTATTCCCCCCATA[C/G]ATATATAATTTAGCT | 146845 |
| rs192230550 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585305 | AAGATGTGATTACTA[A/G]ATGAACGTTTTTGTC | 146845 |
| rs192274901 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9613371 | CTTTGGTGAGATTCA[C/T]TTCATGAAGTTGGTC | 146845 |
| rs192449791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9614311 | CAGGCATGTGCCACC[A/G]CGCCCAGCTAATTTT | 146845 |
| rs192457104 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9581258 | GAAGTGCTGGTTGCA[C/T]AGCATTGTGAATGCA | 146845 |
| rs192460529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9629319 | AAAACAGTAATTTCT[C/T]AGTATTGTCTTATGC | 146845 |
| rs192460819 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP52 | GRCh38.p7 | 17:9606134 | ATGCCTGTAATCTTA[A/G]CGCTTTGGGAGGCCA | 146845 |
| rs192463425 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9580983 | ATAATAGCTGAAACA[C/T]TGGAAGAAACAACCC | 146845 |
| rs192605413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9611426 | GGGATGAGATTGTGA[C/T]TCACTGCAGCCTCCA | 146845 |
| rs192610899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642659 | ATAAATGCATGAAAT[A/G]AATTAAGTTTCACAA | 146845 |
| rs192630659 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9578301 | CTTTTCAGGACATGA[C/T]GGCACGTTAAGTGGG | 146845 |
| rs192731182 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9602284 | CTTTTCTAGCCCCCA[A/C]CCCTGACAGGCCCCG | 146845 |
| rs192777467 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638442 | ACAGGGTGACCTGAA[A/G]TCTGTTTTGAAGAAA | 146845 |
| rs192782894 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | CFAP52 | GRCh38.p7 | 17:9595167 | GGTTAAATATGAATT[G/T]TAGAAATCCTTTTTT | 146845 |
| rs192846280 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | CFAP52 | GRCh38.p7 | 17:9629399 | TCACATCAATGAAAA[G/T]TTCAGTGGATCTTTA | 146845 |
| rs192890596 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585459 | GGATCACGAGGTCAG[C/G]AGTTCAAGACCAGCC | 146845 |
| rs192928435 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9626940 | AGACATTGCTTGAGA[G/T]GTACTGAAATCTAAA | 146845 |
| rs193109697 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9639233 | TCAGGAGTTCGAGAC[C/G]AGCCTAGCCAACATG | 146845 |
| rs193248334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9587459 | CCCTGCTTTCCACAA[C/T]GGTTCAACTAATCTA | 146845 |
| rs193264352 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9614968 | AAACTATTAGCACAG[G/T]TAGAAAGAGTTTATT | 146845 |
| rs199520473 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9597803 | TGGGACTCTGTCAGA[A/G]AGAGAGAGAGAGAGA | 146845 |
| rs199527065 | in-del | -/T | 0.0125133 | 0.0781029 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598216 | GATTGTGGTTTTTTG[-/T]TTTTTTTTTTTACAT | 146845 |
| rs199546964 | snp | A/G | 0.493568 | 0.0563433 | intron-variant | CFAP52 | GRCh38.p7 | 17:9591227 | TTTTTAGTAGAGACG[A/G]GGGTCTCTTCATGTT | 146845 |
| rs199611903 | snp | C/G | 3.2969e-05 | 0.00405998 | missense, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643133 | ATAAGTCCAGGAAAT[C/G]AATATATTGTTAGTG | 146845 |
| rs199655962 | snp | A/G | 5.01777e-05 | 0.00500863 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9598297 | GCCAACTGAGTGCCA[A/G]ACAGGACAGTTGAAA | 146845 |
| rs199767401 | in-del | -/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9594894 | GCAAATTAGGGAGGG[-/T]TTTTTTTTTTTTTTT | 146845 |
| rs199769459 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632037 | CTTGGCCTCCCAAAG[C/T]GCTGGGATTACAGGT | 146845 |
| rs199772187 | snp | C/T | 0.000148379 | 0.00861205 | intron-variant, synonymous-codon | CFAP52 | GRCh38.p7 | 17:9585939 | GTCTGGAGAGTACAT[C/T]GCCTCCGGACAAGTC | 146845 |
| rs199782280 | snp | C/T | 0.00010612 | 0.00728344 | intron-variant | CFAP52 | GRCh38.p7 | 17:9608267 | TAGAGACCCACTAAA[C/T]GGAGATTTGCTTAAA | 146845 |
| rs199797578 | in-del | -/AGAAAGAAAGAAAG | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631069 | GAAAGAAAGAAAGAA[-/AGAAAGAAAGAAAG]AGAAAGAAAGAAAGA | 146845 |
| rs199856158 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631024 | AGAAAGAAAGAAAGA[A/G]AGAAAGAGAGAGAGA | 146845 |
| rs199938332 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9619288 | CACATACACTCTCCC[A/G]AGACTAAACCAGGAG | 146845 |
| rs199988393 | snp | C/T | 0.000399281 | 0.0141238 | missense | CFAP52 | GRCh38.p7 | 17:9628761 | TGCTGCGGATCACCG[C/T]GCCCAACATGACCTG | 146845 |
| rs200034671 | in-del | -/AAG | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636193 | AAAAAGAAAGAAAGA[-/AAG]AAAGAAAGAAAGAAA | 146845 |
| rs200054366 | snp | G/T | | | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9633021 | GGTCATCAGTGGCGG[G/T]GGGGAAGGGGAGGTA | 146845 |
| rs200087214 | snp | G/T | 0.0332751 | 0.124621 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598216 | GATTGTGGTTTTTTG[G/T]TTTTTTTTTTTACAT | 146845 |
| rs200112676 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631036 | AGAAAGAAAGAGAGA[A/G]AGAGAGAGAGAGAGA | 146845 |
| rs200147444 | in-del | -/TT | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9640442 | TGTTGTTTCCCCACG[-/TT]TGTCCATCTCTTTTC | 146845 |
| rs200153894 | snp | C/T | 0.000266347 | 0.011537 | missense, upstream-variant-2KB, utr-variant-5-prime | CFAP52, STX8 | GRCh38.p7 | 17:9576721 | AAATTTCGCCGGAGG[C/T]CCAAGTGGCGGAGCT | 146845 |
| rs200206387 | snp | A/C/G | 1.67584e-05 | 0.00289464 | missense | CFAP52 | GRCh38.p7 | 17:9608219 | GCTACAAACCCATCA[A/C/G]GTAAGTTCCGGGTCT | 146845 |
| rs200227649 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631086 | AAAGAAAGAAAGAGA[A/G]AGAAAGAAAGAGAAA | 146845 |
| rs200234895 | snp | A/G | 9.8894e-05 | 0.00703116 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9638675 | GTGCTATCACCCTGA[A/G]GAGTTCCAGATCATC | 146845 |
| rs200263409 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9610690 | CAGGTGCCCGCCACC[A/G]AGCCCAGCTAATTTT | 146845 |
| rs200272706 | in-del | -/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9581416 | ATAGATGTATATAAA[-/C]TAATGAGGAAAGATG | 146845 |
| rs200291588 | snp | A/G | 0.00199801 | 0.0315438 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586859 | TAAACATAGTTACTT[A/G]TTTTCTTTATTTTTT | 146845 |
| rs200298733 | in-del | -/A | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9640227 | GGTCAAGCACTCTTT[-/A]TTTTTTTTTTTTTTT | 146845 |
| rs200308260 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9608094 | AGATTTTTGTGCTTT[G/T]TCTTAACACAGTTTT | 146845 |
| rs200319536 | snp | C/T | 4.94417e-05 | 0.00497176 | missense, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643115 | AACATCACACGCATC[C/T]GCATAAGTCCAGGAA | 146845 |
| rs200330236 | in-del | -/TT | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9614158 | TCTTTTCTTTCTTTC[-/TT]TTTTTTTTTTTTTTT | 146845 |
| rs200347632 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9602664 | TCAAATGGTATTTCT[A/G]GTTCTAGATCCTTGA | 146845 |
| rs200419384 | snp | A/G | 0.00199792 | 0.0315431 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9635473 | GGAACACAAGTCATC[A/G]GTGTCCTGCATTAGG | 146845 |
| rs200446286 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9618499 | TCTGCACCAAGCAGA[C/T]CTAATAGACATCTAC | 146845 |
| rs200456785 | in-del | -/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9596720 | TTGTGTGTGTGTGTG[-/T]TGTTTTTTTTTTGAG | 146845 |
| rs200491346 | snp | A/G | 0.000160218 | 0.00894893 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575821 | CATCCTGCAGACTCC[A/G]CCCGCCGCTCGGACT | 146845 |
| rs200492665 | snp | A/G | 0.000132613 | 0.00814179 | missense | CFAP52 | GRCh38.p7 | 17:9633014 | GTAAAAGGGTCATCA[A/G]TGGCGGTGGGGAAGG | 146845 |
| rs200546540 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9623667 | AGAACTTTGCTTAGC[-/T]TTTTTTGTTTGTTTG | 146845 |
| rs200599582 | in-del | -/AGAAAG | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631077 | GAAAGAAAGAAAGAA[-/AGAAAG]AGAAAGAAAGAAAGA | 146845 |
| rs200620442 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CFAP52 | GRCh38.p7 | 17:9580758 | GCAAAGGCAAAAAAA[A/G]AAAAAAAAAGGGTAA | 146845 |
| rs200652970 | in-del | -/TTTCT | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9629492 | TTCTTTCTTTCTTTC[-/TTTCT]TTTCTTTTCTTTCTT | 146845 |
| rs200662970 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9597831 | AGAGAGAGAGAGAGA[A/G]AGAGAGAAAGAGAGA | 146845 |
| rs200721846 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9604802 | AAATAAATAAATAAA[A/T]AAAAGAAGATATACA | 146845 |
| rs200770987 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9640228 | GGTCAAGCACTCTTT[A/T]TTTTTTTTTTTTTTT | 146845 |
| rs200795740 | in-del | -/AAAT | 0.475789 | 0.107327 | intron-variant | CFAP52 | GRCh38.p7 | 17:9604751 | CAAGACTCTGTCTCA[-/AAAT]AAATAAATAAATAAA | 146845 |
| rs200804897 | snp | C/T | 3.30759e-05 | 0.00406655 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600053 | GCCAAGATTTCTTTT[C/T]CTTGCTTCTTCAGGT | 146845 |
| rs200948001 | in-del | -/T | 0.0479149 | 0.147179 | intron-variant | CFAP52 | GRCh38.p7 | 17:9613984 | TCACTTTTTCCCCTC[-/T]TTTTTTTTTAATAAG | 146845 |
| rs200953170 | snp | C/T | 6.59217e-05 | 0.00574078 | missense | CFAP52 | GRCh38.p7 | 17:9612445 | CTCATAGCGACTTGT[C/T]ACTTTGATGCTGTCG | 146845 |
| rs200985528 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9584600 | CTCTTTTAGCAGATT[A/T]ATGCAGTATTTTTTT | 146845 |
| rs200987134 | in-del | -/AAGAAAG | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636193 | AAAAAGAAAGAAAGA[-/AAGAAAG]AAAGAAAGAAAGAAA | 146845 |
| rs201000246 | snp | C/T | 0.00109667 | 0.0233908 | utr-variant-3-prime, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643243 | TTGCACGCAGTCCTG[C/T]TGAAGACTGAGTTTA | 146845 |
| rs201045232 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9619700 | GGCTGGTTCAATATA[C/T]GCAAATCAATAAATG | 146845 |
| rs201064550 | snp | A/G | 0.000589069 | 0.0171519 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643006 | AGCAATGCCATATAC[A/G]TGTTTATCTTTTTCA | 146845 |
| rs201071925 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9621095 | GAGAAAATTTTCGCA[A/G]CCTACTCATCTGACA | 146845 |
| rs201082194 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631082 | AAAGAAAGAAAGAAA[A/G]AGAAAGAAAGAAAGA | 146845 |
| rs201094305 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9617883 | ACAACCGGTACCAGC[C/T]GCTGCAAAATCATGC | 146845 |
| rs201154947 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9589816 | CTTTTTTTTTTTTTT[G/T]CAAGCAGAAAAAGCC | 146845 |
| rs201281766 | in-del | -/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9629495 | TTTCTTTCTTTCTTT[-/C]TTTTCTTTTCTTTCT | 146845 |
| rs201320583 | in-del | -/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9614174 | TTTTTTTTTTTTTTT[-/T]GAGACTGAGTCTCGC | 146845 |
| rs201352201 | snp | C/T | 0.000115336 | 0.00759305 | missense | CFAP52 | GRCh38.p7 | 17:9612389 | TAGGAACAGAAGAAT[C/T]GCACATTTATCGTGT | 146845 |
| rs201386192 | snp | C/T | 0.00199792 | 0.0315431 | missense | CFAP52 | GRCh38.p7 | 17:9598280 | CCAAATAGAAAAATC[C/T]GGCCAACTGAGTGCC | 146845 |
| rs201479202 | snp | A/G | 0.000148274 | 0.008609 | intron-variant, missense | CFAP52 | GRCh38.p7 | 17:9585901 | GGTCATGGCAACAAC[A/G]TCTCCTGCTTGGCCA | 146845 |
| rs201487824 | in-del | -/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9627113 | TTTTTTTTTTTTTTT[-/T]GAGCTTGACAGACAA | 146845 |
| rs201492544 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9587120 | TAAGAACCTGTGGTA[-/T]TTGGTTTTCTACTCC | 146845 |
| rs201508680 | in-del | -/A | 0.0603597 | 0.1629 | intron-variant | CFAP52 | GRCh38.p7 | 17:9606070 | ACCTAAAACTGCTCT[-/A]AAAAAAAATAGCCTA | 146845 |
| rs201511097 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636195 | AAAGAAAGAAAGAAA[A/G]AAAGAAAGAAAGAAA | 146845 |
| rs201604779 | snp | C/T | 3.3189e-05 | 0.0040735 | missense | CFAP52 | GRCh38.p7 | 17:9608125 | TCCCCCTAGGGAGTG[C/T]CAGCTATCAGGTGCC | 146845 |
| rs201635440 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9618196 | AAAGGCAGGGGTTGC[A/G]ATCCTAGTCTCTGAT | 146845 |
| rs201716592 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9629561 | GCTTTTTTTTTTTTT[C/T]TCTCAGATGGAGTTT | 146845 |
| rs201765793 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9597839 | AGAGAGAAAGAGAGA[A/G]AGAGAGAGAGAAAGA | 146845 |
| rs201767852 | snp | C/T | 9.89707e-05 | 0.00703389 | missense, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643143 | GAAATCAATATATTG[C/T]TAGTGTAAGTGCCGA | 146845 |
| rs201768867 | snp | A/C/T | 0.00013198 | 0.0081225 | intron-variant | CFAP52 | GRCh38.p7 | 17:9635367 | TCCCTTCAGAAGTCC[A/C/T]AAGTGTGGATCAAGA | 146845 |
| rs201777194 | snp | C/T | 4.94262e-05 | 0.00497098 | intron-variant, synonymous-codon | CFAP52 | GRCh38.p7 | 17:9585900 | GGGTCATGGCAACAA[C/T]GTCTCCTGCTTGGCC | 146845 |
| rs201809375 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CFAP52 | GRCh38.p7 | 17:9580757 | GGCAAAGGCAAAAAA[A/G]GAAAAAAAAAGGGTA | 146845 |
| rs201825631 | in-del | -/AAGAAAGAAAGAAAGAAAG | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636193 | AAAAAGAAAGAAAGA[-/AAGAAAGAAAGAAAGAAAG]AAAGAAAGAAAGAAA | 146845 |
| rs201868257 | snp | A/G | 0.00340601 | 0.0411267 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600021 | GCTGATATTACAGGC[A/G]TGAGCCACCGAGGCT | 146845 |
| rs201871247 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9594890 | ATTAGCAAATTAGGG[A/G]GGGTTTTTTTTTTTT | 146845 |
| rs201872577 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631084 | AGAAAGAAAGAAAGA[A/G]AAAGAAAGAAAGAGA | 146845 |
| rs201896769 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | CFAP52 | GRCh38.p7 | 17:9594892 | TAGCAAATTAGGGAG[A/G]GTTTTTTTTTTTTTT | 146845 |
| rs201932551 | snp | G/T | 8.29002e-05 | 0.00643764 | intron-variant | CFAP52 | GRCh38.p7 | 17:9628869 | TCTAGCTGCGGTTTT[G/T]ATTCTTGTCACTCTC | 146845 |
| rs201951404 | in-del | -/AGAAAGAAAGAG | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636242 | GAAAGAAAGAAAGAA[-/AGAAAGAAAGAG]AAAGAAAAATAACTA | 146845 |
| rs201954429 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9610544 | CCATTTTTTTTTTTT[G/T]TTTGTTTTGAGATGG | 146845 |
| rs202001632 | in-del | -/AAAT | 0.0349115 | 0.127424 | intron-variant | CFAP52 | GRCh38.p7 | 17:9578094 | AGACTCCGTCTCAAA[-/AAAT]AAATAAATAAATAAA | 146845 |
| rs202035421 | snp | A/G | 3.29462e-05 | 0.00405857 | intron-variant, missense | CFAP52 | GRCh38.p7 | 17:9585806 | TCAAATGCCATCCTG[A/G]CCAGGAGCATATGAT | 146845 |
| rs202069537 | snp | A/G | 0.000416566 | 0.014426 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641867 | GAAAAAGCCAAGCCT[A/G]GCTTATTTAGACGAG | 146845 |
| rs202088911 | snp | C/T | 0.00199806 | 0.0315443 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9632991 | CGCCATCGCCACCAC[C/T]AGTGACTGTAAAAGG | 146845 |
| rs202132510 | snp | C/T | 0.000197733 | 0.00994119 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9594247 | TGGCAGCCCTGCAGC[C/T]GGCCTCAATGTTGGC | 146845 |
| rs202134055 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9585574 | TACTCGGGAGGCTGA[A/G]GCAGGAGAATCACTT | 146845 |
| rs202134805 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9620386 | GAACATTCCATGCTC[A/G]TGGGTAGGAAGAATC | 146845 |
| rs202173516 | in-del | -/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9596722 | TGTGTGTGTGTGTGT[-/G]TTTTTTTTTTGAGAT | 146845 |
| rs202181991 | in-del | -/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9632387 | TTATAGATATAAGCC[-/T]TTTTTTTTTAAATAA | 146845 |
| rs202195834 | in-del | -/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9610710 | AGCTAATTTTTTTTT[-/T]GTATTTTTAGTAGAG | 146845 |
| rs267605111 | snp | A/G | | | missense | CFAP52 | GRCh38.p7 | 17:9598272 | TGGATCTTCCAAATA[A/G]AAAAATCTGGCCAAC | 146845 |
| rs367551679 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9602397 | TTCTGTTCCTGTTTT[A/G]GTTTGCTGAGAATGA | 146845 |
| rs367587023 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631489 | TATGAGAGGGTGCCA[A/G]CCATTTGAAGACCTG | 146845 |
| rs367598134 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9624669 | CAGTACCTGGGTCTA[C/G]TTGGAATCAGTTGCT | 146845 |
| rs367619223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586335 | TTGGGAGGCCTAGAC[A/G]GTCGGATCCCCTGAG | 146845 |
| rs367635238 | snp | C/T | 0.000207232 | 0.0101771 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575759 | CCTCCCCGAAGGTCC[C/T]TCCACGCACCGCCGC | 146845 |
| rs367666001 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9625803 | ATCCAGTTTTTCTAA[C/T]TGTTATTTGTGAGAA | 146845 |
| rs367669298 | snp | C/T | 0.000103484 | 0.00719245 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633063 | AATTTGAAAAAATAA[C/T]GCTCTGTTTAGAACA | 146845 |
| rs367677970 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9577964 | GGGCGTGGTGGTAGG[A/T]GCCTGTAATCCCAGC | 146845 |
| rs367699122 | snp | A/G | 4.97467e-05 | 0.00498707 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600037 | TGAGCCACCGAGGCT[A/G]GCCAAGATTTCTTTT | 146845 |
| rs367749855 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9580818 | TCAATTACTACTGCC[A/G]GTATTAATTTTACAA | 146845 |
| rs367753847 | snp | C/G | 1.66468e-05 | 0.00288498 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641864 | TAGGAAAAAGCCAAG[C/G]CTGGCTTATTTAGAC | 146845 |
| rs367781619 | snp | A/G | 0.00066788 | 0.0182618 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638737 | CCAGTGAGAGATGAG[A/G]TCTTTCCAGCGCAAG | 146845 |
| rs367783574 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586670 | TTTAATGCCTCCCTA[C/T]GATCTGACGGTGTGT | 146845 |
| rs367791419 | snp | C/G | 1.65094e-05 | 0.00287305 | missense | CFAP52 | GRCh38.p7 | 17:9628717 | CAAGAAGGATATCAG[C/G]GTGTGGCACACATCA | 146845 |
| rs367800826 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9574800 | CGGCCTCCCAAAGTA[C/G]TGGGATTACAGGCGT | 146845 |
| rs367809736 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9620077 | GTCCCTGTTTGCAGA[C/T]GACATGATTGTTTAT | 146845 |
| rs367875400 | snp | A/C | 0.000197716 | 0.00994078 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600207 | AGACCATCGCCACTG[A/C]CCTGCCATTTTTCTC | 146845 |
| rs367879592 | snp | A/G | 1.64855e-05 | 0.00287097 | missense | CFAP52 | GRCh38.p7 | 17:9632954 | TGTATGTCATTAACA[A/G]TGCTCACAGGATCGG | 146845 |
| rs367965417 | in-del | -/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9580458 | TTGGGAGGTTGAGGC[-/C]AGGAAGATTCCTTGA | 146845 |
| rs367968290 | in-del | -/T | 0.00309707 | 0.0392294 | intron-variant | CFAP52 | GRCh38.p7 | 17:9594162 | TGTTTTCTCTTTGAC[-/T]TTTTTTTTTTGGTCC | 146845 |
| rs368103127 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9604799 | AATAAATAAATAAAT[A/G]AATAAAAGAAGATAT | 146845 |
| rs368229972 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9628916 | TACATGTGGATAACC[C/T]AGAACAGCCTCCCAC | 146845 |
| rs368259748 | in-del | -/AG/AGAG | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9597803 | GGGACTCTGTCAGAA[-/AG/AGAG]AGAGAGAGAGAGAGA | 146845 |
| rs368262549 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9594165 | TTTCTCTTTGACTTT[G/T]TTTTTTTGGTCCCTC | 146845 |
| rs368266408 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CFAP52 | GRCh38.p7 | 17:9640210 | TTTGCACTCCTGATT[C/T]CTGGTCAAGCACTCT | 146845 |
| rs368310731 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | CFAP52 | GRCh38.p7 | 17:9628632 | TGCATCTGGGAAACT[C/G]CATCTTTTATGGTTG | 146845 |
| rs368322610 | snp | C/T | 0.000167591 | 0.00915246 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641879 | CCTGGCTTATTTAGA[C/T]GAGGACATGGAAGGA | 146845 |
| rs368337134 | in-del | -/AA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631027 | AAGAAAGAAAGAAAG[-/AA]AGAGAGAGAGAGAGA | 146845 |
| rs368345042 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9586560 | AAAAGAGTGAGACTC[C/T]GTCTCAACAAAAAAA | 146845 |
| rs368368506 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631151 | GCTCAAAAGTCTTTT[A/G]CCCTCTAAGAGTAAA | 146845 |
| rs368369204 | snp | G/T | 1.75748e-05 | 0.00296431 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586850 | GTAATGAACTAAACA[G/T]AGTTACTTATTTTCT | 146845 |
| rs368404065 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | CFAP52 | GRCh38.p7 | 17:9601128 | GGACATGGATGAAGC[-/T]GGATACCATCATTCT | 146845 |
| rs368425154 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CFAP52 | GRCh38.p7 | 17:9593990 | CAATAACAACAACAA[A/C]AAAAAACTTTTAATG | 146845 |
| rs368432792 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9609158 | CTGTCTTCATTCCAA[G/T]AAATCTGTGTTGAAC | 146845 |
| rs368437264 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9641280 | GAGGAAGAGGGAGGG[C/T]GCAGTCCCAGTGGGA | 146845 |
| rs368445469 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9627142 | TGAGCTTGACAGACA[A/G]AAGAAGGGTTTTGGG | 146845 |
| rs368466692 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9581516 | AAGTGTACATATGTT[C/T]GAGAGAGAGAGAGGG | 146845 |
| rs368507611 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9606386 | CCTGTCTCCAAAATA[C/T]ACACACACACACACA | 146845 |
| rs368527273 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9592631 | ATATGTGGTCTTTTG[A/T]GACTGGCTTCTTTCA | 146845 |
| rs368543439 | snp | C/G | 6.59968e-05 | 0.00574404 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9586751 | GCTTGCTCGGCTGTC[C/G]CTTCACAAAGGCAAA | 146845 |
| rs368545420 | in-del | -/AA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631067 | GAGAAAGAAAGAAAG[-/AA]AGAAAGAAAGAAAGA | 146845 |
| rs368549775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9603796 | CCTATGTAACAAACC[C/T]GCATGTTCTGCACAT | 146845 |
| rs368596154 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9600466 | TAGGCTAATCTTGAA[C/T]TCCTGACCTCAAGTG | 146845 |
| rs368606327 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9596103 | TATATATATATATAT[A/G]TACACATATAGAGAG | 146845 |
| rs368658792 | snp | A/C/T | 4.96465e-05 | 0.00498209 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641844 | GTCACAGGTTAGTCC[A/C/T]GGGATAGGAAAAAGC | 146845 |
| rs368707227 | snp | A/G | 1.64806e-05 | 0.00287054 | missense | CFAP52 | GRCh38.p7 | 17:9612446 | TCATAGCGACTTGTC[A/G]CTTTGATGCTGTCGA | 146845 |
| rs368769737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9604597 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 146845 |
| rs368773719 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CFAP52 | GRCh38.p7 | 17:9589673 | GGGAGGCGGAGGTTG[C/T]AGTGAGCCAAGGTTG | 146845 |
| rs368879860 | snp | C/T | 0.000346486 | 0.0131576 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9638696 | CCAGATCATCACCAG[C/T]GGAACAGACAGAAAG | 146845 |
| rs368907834 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9578577 | TTATTTATTTTGAGA[C/T]GGTGGAGTCTCGCTC | 146845 |
| rs368919049 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9615782 | CCCAGCTAATTAAAA[A/C]AAAAAAAAAATTCTT | 146845 |
| rs368929025 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9598692 | CTTGAACCTGGGAGG[C/T]GGAAGTTGCGGTGAG | 146845 |
| rs368988398 | snp | A/G | 0.000164764 | 0.00907495 | missense | CFAP52 | GRCh38.p7 | 17:9594255 | CTGCAGCCGGCCTCA[A/G]TGTTGGCAATGCCAC | 146845 |
| rs369013852 | snp | A/T | 4.9611e-05 | 0.00498026 | intron-variant | CFAP52 | GRCh38.p7 | 17:9628854 | GATCTGGCTTGGGGC[A/T]CTAGCTGCGGTTTTG | 146845 |
| rs369024546 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9604500 | CAGCCGGGCGCAGTG[C/G]CTTGTGCCTGTAATC | 146845 |
| rs369069310 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636492 | AGGAGTAACTCAAAG[A/G]ATTTTTGAACAGTGG | 146845 |
| rs369072027 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9583817 | AAACATATTACAAGG[C/G]TTTATAATTGTTGAG | 146845 |
| rs369073779 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9597562 | GTAATCCCAGCACTT[G/T]GGGAGGCTGAAGCGG | 146845 |
| rs369076868 | in-del | -/CA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9610013 | AGAGAGAGAGAGAGA[-/CA]GAGACAGAGAGAGAC | 146845 |
| rs369133428 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9629091 | AAATTTAGAAGTTCA[A/G]TTTTGAAAAGGAGTT | 146845 |
| rs369316395 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9595528 | TTTGCAGAGTGATTT[G/T]ACTAAGCCAGGGTTT | 146845 |
| rs369328779 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9606240 | TTTTTAAAAATTAGC[C/T]GGCGTGGTGGCATGC | 146845 |
| rs369400693 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9588790 | TTTTTTTTTTTTTTT[G/T]AGATGGAGTTTCACT | 146845 |
| rs369440206 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9584991 | AGACATGGATTAACC[A/T]GGAGAATATTATGCT | 146845 |
| rs369482442 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9584881 | GCCTGCCTCGGCCTC[C/G]CAAGTGCTGGGATTA | 146845 |
| rs369608384 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9609250 | AGATGAAAAAAAAAA[C/T]CCCTGTCCTCATGGA | 146845 |
| rs369620992 | snp | A/C/T | 0.000396659 | 0.0140783 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638598 | TCACAGCTTTTGAAT[A/C/T]TACTTTCCAGGCGTC | 146845 |
| rs369625026 | in-del | -/TT/TTT | 0.0117611 | 0.0757776 | intron-variant | CFAP52 | GRCh38.p7 | 17:9596722 | GTGTGTGTGTGTGTG[-/TT/TTT]TTTTTTTTTTGAGAT | 146845 |
| rs369631577 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9630221 | CTCTTCTCACCCAGT[A/T]TACTTTCCCGCAGTC | 146845 |
| rs369634065 | snp | C/T | 4.94271e-05 | 0.00497102 | stop-gained | CFAP52 | GRCh38.p7 | 17:9612349 | ACTTCTATCACACTT[C/T]GAGGAGAAGGACACC | 146845 |
| rs369670327 | in-del | -/A | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9604183 | GACCTAAAACACAAA[-/A]CAATAGAACTCCTGA | 146845 |
| rs369683878 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | CFAP52 | GRCh38.p7 | 17:9590464 | AGGCAAGCCCCTTCT[A/G]AAGCCCAAACATTCT | 146845 |
| rs369714818 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9630106 | CTCATTTCAAAGTAC[A/G]TCCAAGGTCCCTCAC | 146845 |
| rs369729611 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9613062 | ATTAAGTGCATTTTC[A/G]ACTTAGGATATTTTC | 146845 |
| rs369740067 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB, intron-variant | CFAP52, USP43 | GRCh38.p7 | 17:9643797 | AAGAAAATGTGTGGT[A/G]TTGGGGATCTCAGGA | 146845 |
| rs369770347 | snp | C/T | 3.29592e-05 | 0.00405938 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9628786 | GACCTGCCACGGCAT[C/T]GACTTCATGAGGGAC | 146845 |
| rs369821312 | snp | A/G | 3.41839e-05 | 0.0041341 | utr-variant-5-prime, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576645 | ACCATAACGACCAGA[A/G]GACGCTGCAGCCACT | 146845 |
| rs369864048 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9638495 | AGTATGAGATGTTTG[A/G]CATGGAGATAAACCA | 146845 |
| rs369866944 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9578857 | AGCCACAGGGTGGAG[A/G]GGTGCATGGCCTTAG | 146845 |
| rs369869044 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9600825 | ATAAAAAGTCAGTGA[C/T]GGACCCAAAGCCACA | 146845 |
| rs369875670 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9627744 | TTAGAGGCAAATTCT[C/T]TTGTCTCACTCTGTC | 146845 |
| rs369876242 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9627278 | ACTTTGGGAGGCCGA[A/T]GTGGGTGGATCACCT | 146845 |
| rs369992887 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9603969 | TAGATAAATGGATCA[A/G]TGGGACAGAATAGAG | 146845 |
| rs369998975 | snp | C/T | | | downstream-variant-500B, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643477 | TGTTTTCTGCAACTC[C/T]GCAAAACCCACAGAC | 146845 |
| rs370021939 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9607143 | TTCAGGTGAGGAGTT[C/T]GAGACCAGCCTGGCC | 146845 |
| rs370034154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9591313 | AAAGTGCTGAGATTA[C/T]AGGCTTGAGTCGCCG | 146845 |
| rs370036848 | snp | A/T | 9.88598e-05 | 0.00702995 | missense | CFAP52 | GRCh38.p7 | 17:9594274 | TGGCAATGCCACCAA[A/T]GTGATCTTCTCCAGG | 146845 |
| rs370066940 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9611655 | ACAGGCATGAACAAC[G/T]GTACAAGCTCTGAAA | 146845 |
| rs370139274 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9626065 | GTGGGAGAGAGGGAG[C/G/T]ACATGGGCTTGGTAC | 146845 |
| rs370163534 | snp | C/T | 3.33078e-05 | 0.00408078 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641866 | GGAAAAAGCCAAGCC[C/T]GGCTTATTTAGACGA | 146845 |
| rs370231741 | snp | A/G | 3.30786e-05 | 0.00406672 | missense, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643157 | GTTAGTGTAAGTGCC[A/G]ATGGAGCCATTTTGC | 146845 |
| rs370232975 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633055 | AAAGCAGAAATTTGA[A/G]AAAATAACGCTCTGT | 146845 |
| rs370255754 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9595755 | TAAAATTTTTGACAT[A/G]GCACCTATGTATGCT | 146845 |
| rs370297079 | snp | A/G | 8.23879e-05 | 0.00641772 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9612414 | TCGTGTCAGCTTCAC[A/G]GATTTCAAAGAGACG | 146845 |
| rs370342034 | snp | A/T | 1.70075e-05 | 0.00291607 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598375 | ACAATTAGCACACGT[A/T]CCTGTTAGCAGTGCT | 146845 |
| rs370394610 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9591319 | CTGAGATTATAGGCT[C/T]GAGTCGCCGCTCCCG | 146845 |
| rs370432867 | in-del | ATT/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9594893 | AGCAAATTAGGGAGG[ATT/G]TTTTTTTTTTTTTTT | 146845 |
| rs370442957 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9578168 | ATGAATACTCATGAA[A/G]GTGGTCCCAACACAT | 146845 |
| rs370444802 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9599616 | ACCCATCTTTGAGCC[C/T]GGGGAAATAGAAGCA | 146845 |
| rs370454094 | snp | G/T | 8.50651e-05 | 0.00652114 | utr-variant-5-prime, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576666 | TGCAGCCACTAGGGA[G/T]GAGAGCAAAGTAATC | 146845 |
| rs370564522 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9627796 | CACGATCATAGCTCA[A/G]TGCAGTCTCCAACCC | 146845 |
| rs370697977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586291 | AGAGCGGGCTGGGCG[C/T]GGTGGCTCATGCCTG | 146845 |
| rs370701311 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9589817 | TTTTTTTTTTTTTTG[C/T]AAGCAGAAAAAGCCT | 146845 |
| rs370711179 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9598031 | CTGTGTTCAAGCTCC[A/G]CACTTTCTAATTTGG | 146845 |
| rs370740585 | snp | C/T | 0.00177333 | 0.029724 | utr-variant-3-prime, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643233 | AGCCTTGGCGTTGCA[C/T]GCAGTCCTGTTGAAG | 146845 |
| rs370755204 | snp | A/G | 1.66136e-05 | 0.00288211 | intron-variant | CFAP52 | GRCh38.p7 | 17:9612505 | GAGAAAAACAAGAAT[A/G]TGGAGATTTGATGCA | 146845 |
| rs370813607 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9612408 | CATTTATCGTGTCAG[C/T]TTCACGGATTTCAAA | 146845 |
| rs370814544 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9603717 | CCTAATGTAGATGAC[A/G]GGTAATATAGATGAT | 146845 |
| rs370833922 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638762 | CGCAAGAGAAAAGCA[C/G]TGAGGCGTTGTGGTG | 146845 |
| rs370836296 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9640739 | ACTTTCACCTCCTGG[G/T]TACAAGTGATTCTCA | 146845 |
| rs370851417 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9592465 | CAAGAGCAAAACTCC[A/G]TCTCAAAAAAATTAA | 146845 |
| rs370857457 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9619546 | GGGCAGAGACACAAC[A/C]AAAAAAGAGAATTTT | 146845 |
| rs370902588 | snp | G/T | 1.65018e-05 | 0.00287239 | missense, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641827 | AGGAAGGGGTGCACT[G/T]TGTCACAGGTTAGTC | 146845 |
| rs370915625 | snp | A/G | 0.000163987 | 0.00905353 | missense, upstream-variant-2KB, utr-variant-5-prime | CFAP52, STX8 | GRCh38.p7 | 17:9576756 | CTTGACGCCGTGATC[A/G]GCTTCAATGGTGAGG | 146845 |
| rs370935367 | in-del | -/AA/AAAGAAAGAA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631052 | GAGAGAGAGAGAGAG[-/AA/AAAGAAAGAA]AGAAAGAAAGAAAGA | 146845 |
| rs370941616 | snp | G/T | | | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641988 | ACTGCAGCCAATGTG[G/T]CTGAGAAAGAAAAAT | 146845 |
| rs370941869 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9579553 | ACTGAAACTCACTAT[A/T]GTGTTACATTATTCA | 146845 |
| rs370973140 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9586079 | AATGTGCTTTATTCT[A/T]CCTTCTTCTTCTTTT | 146845 |
| rs371070702 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9630902 | GAGACAGGAGAGTTT[C/T]TTGAACCCGGGAGGT | 146845 |
| rs371088330 | snp | A/G | 0.00013338 | 0.00816531 | intron-variant | CFAP52 | GRCh38.p7 | 17:9594364 | AACTCATAAATTGCT[A/G]TATTTTCTTGCACAG | 146845 |
| rs371106587 | in-del | -/ACGCTCCTGCCTCAGCCTCCCAAGTATCTGGGACTACAGGC | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9629693 | GCTGGGATTACAGGC[lengthTooLong]GTGTGTCATCACGAT | 146845 |
| rs371149762 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9598760 | AGTGACACTCTGTTT[A/C]AAAAAAAAAAGAAGA | 146845 |
| rs371164640 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9622065 | TAACCAATGTTTGTA[C/T]CTAATCTGCCAAAAA | 146845 |
| rs371166736 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9619787 | GCAGAAAAAGCCTTT[C/G]ACAAAATTCAACAAC | 146845 |
| rs371190727 | snp | A/C | 8.27493e-05 | 0.00643178 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600048 | GGCTGGCCAAGATTT[A/C]TTTTTCTTGCTTCTT | 146845 |
| rs371226604 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9581179 | AAAATTAGCCGGGCG[C/T]GGTGGCGGGCACCTG | 146845 |
| rs371231134 | snp | A/G | 8.28686e-05 | 0.00643641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585986 | AGGTGAATACAGTGA[A/G]AACGACTCATTGTCA | 146845 |
| rs371271335 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9580225 | GTTTATGTATTGTCT[A/G]TGGCTGCTTTTATAC | 146845 |
| rs371271955 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9587293 | ATTTGGGTTGATTCC[A/G]TGTCTTTGCTATTGT | 146845 |
| rs371275266 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9602695 | GGAATCACCACACTG[C/T]CTTCCACAATGGCTG | 146845 |
| rs371325603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9631702 | GCACAAATACTAGTT[A/G]CCGTGGAGGATAAAG | 146845 |
| rs371347534 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631154 | CAAAAGTCTTTTACC[C/T]TCTAAGAGTAAATGA | 146845 |
| rs371430166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9624581 | CTATCTGTTCACTTA[C/T]TGATGTGATAGTTTC | 146845 |
| rs371454201 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9577745 | AATTGAGCAGCCTAC[A/T]GTGGGTTGCATAATG | 146845 |
| rs371459662 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9612103 | TGAAGAAGCTTTCCT[G/T]ACTACTTTAACCTAT | 146845 |
| rs371529300 | snp | C/T | 5.10339e-05 | 0.00505117 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586678 | CTCCCTATGATCTGA[C/T]GGTGTGTTCTTGCCC | 146845 |
| rs371539029 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9613316 | ATCAAAAGGAGCTTC[A/G]GTCAGATGTTCTGGT | 146845 |
| rs371551896 | in-del | -/CA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9585669 | AGTGCAAGACTCTGT[-/CA]CACACACACACACAC | 146845 |
| rs371570819 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9592650 | TGGCTTCTTTCACTT[A/T]GCGTAATGTTTTCAA | 146845 |
| rs371613095 | snp | C/T | 3.29603e-05 | 0.00405944 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600220 | TGCCCTGCCATTTTT[C/T]TCCCTTCACTGGCAG | 146845 |
| rs371619273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638113 | TGTACAAATGTGTAC[A/G]TGACATCTTGCTACA | 146845 |
| rs371672007 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9602398 | TCTGTTCCTGTTTTA[G/T]TTTGCTGAGAATGAT | 146845 |
| rs371696052 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9605096 | TGCACTCCTTGCTAT[G/T]TACCCAAAGGAGCTG | 146845 |
| rs371698292 | snp | G/T | 1.6483e-05 | 0.00287076 | missense | CFAP52 | GRCh38.p7 | 17:9628755 | GGGAGCTGCTGCGGA[G/T]CACCGTGCCCAACAT | 146845 |
| rs371704648 | snp | A/C | 0.00187178 | 0.030535 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586864 | ATAGTTACTTATTTT[A/C]TTTATTTTTTTTAAC | 146845 |
| rs371744508 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9589957 | TCTCCTTCTTGGCCC[A/G]GAGGTGCTCTTCACA | 146845 |
| rs371799983 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CFAP52 | GRCh38.p7 | 17:9611420 | AGGGCAGGGATGAGA[C/T]TGTGACTCACTGCAG | 146845 |
| rs371814923 | snp | C/T | 6.58989e-05 | 0.00573978 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9600181 | AAGGACAAATTCAGT[C/T]TGGTGAGTAGAGACC | 146845 |
| rs371817805 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9606827 | CTGCTGAGGCACTTA[C/G]GAAGTTAGGGGTGAG | 146845 |
| rs371873279 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9581593 | GGAGGGAAAGAAGGC[A/G]AGAGAGAGAGAAAAT | 146845 |
| rs371902741 | snp | C/T | 4.94189e-05 | 0.00497062 | intron-variant, missense | CFAP52 | GRCh38.p7 | 17:9585823 | CAGGAGCATATGATT[C/T]ATCCTCTTGGTTGCA | 146845 |
| rs371949441 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9606384 | ACCCTGTCTCCAAAA[A/T]ACACACACACACACA | 146845 |
| rs371979717 | snp | A/G | | | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575228 | AAAAGACTTCATGAT[A/G]TTAACTCAAGAAAGT | 146845 |
| rs371989640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9593244 | GATCCACACCCTATT[C/T]AGTGTAGGATAAAGT | 146845 |
| rs372035567 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9620089 | AGACGACATGATTGT[A/T]TATCTAGAAAACCCC | 146845 |
| rs372058371 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636514 | GAACAGTGGCTTTTT[G/T]AATTTTTGACTATAA | 146845 |
| rs372101059 | in-del | -/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631176 | GTAAATGACAAAGAT[-/C]CCCCCCATCACCTAC | 146845 |
| rs372103458 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600328 | CTCACTGCAACTTCT[A/G]CCTCCCAGGTTCAAG | 146845 |
| rs372107630 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9626681 | AATTTTAAATAAATA[G/T]TAACATTCTAGTGTT | 146845 |
| rs372161491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586898 | TATTTCAGGTTCAGA[C/T]GTACATGTGCAGGTT | 146845 |
| rs372167772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9605423 | TATGGAGACAATAAA[A/G]AGATCAGGCTGGGCG | 146845 |
| rs372195557 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642986 | GTTTCTCTCTCTCCT[A/G]TTGCAGCAATGCCAT | 146845 |
| rs372230830 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9621748 | TCTCAGTAAACTATC[A/G]CAAGAACAAAAAACC | 146845 |
| rs372259143 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9595291 | AGGTACACATGGTTG[G/T]TTACTTTTCCAGCTA | 146845 |
| rs372272286 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CFAP52 | GRCh38.p7 | 17:9602529 | TCCAGTCTATCATTG[A/G]TGGACATTTGGGTTG | 146845 |
| rs372275977 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9603852 | TTTAAAAAAAGAAAG[C/G]ACAATATTGAAGAAG | 146845 |
| rs372332663 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9593948 | CCAGCCTGGGCAACA[A/G]GAGTGAAACTCCATC | 146845 |
| rs372386974 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9601060 | AATGTGGCACATATA[C/T]ACCATGGAATACTAT | 146845 |
| rs372408765 | snp | C/T | 1.6477e-05 | 0.00287024 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9594268 | CAATGTTGGCAATGC[C/T]ACCAATGTGATCTTC | 146845 |
| rs372433899 | in-del | -/TTGCA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9634551 | GACCACGCCATTGCA[-/TTGCA]CTCCAGCCTGGGTGA | 146845 |
| rs372458377 | snp | A/G | 8.34955e-05 | 0.00646071 | missense | CFAP52 | GRCh38.p7 | 17:9586830 | GGAGGCCCAGATGAC[A/G]GAAGGTAATGAACTA | 146845 |
| rs372497486 | in-del | -/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9612801 | GTCCCTGACTTATGA[-/T]TTTTTTTATTTTATG | 146845 |
| rs372593867 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9641071 | TGAATAGATTGTGCA[A/T]TCACAAAGTTTAAGG | 146845 |
| rs372640682 | snp | A/G | 0.000116586 | 0.0076341 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | CFAP52, STX8 | GRCh38.p7 | 17:9576734 | GGCCCAAGTGGCGGA[A/G]CTGGAACTTGACGCC | 146845 |
| rs372735224 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9589701 | TTGTGCCATTGCACT[C/G]CAGCCTGGGGACAAG | 146845 |
| rs372753087 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9580318 | TCTCTGGACCTTTCT[A/T]AAAAAAAAAAAAAAA | 146845 |
| rs372781495 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9627381 | CCAGACATGGTGGCA[C/T]ATGCCTGTAATCCCA | 146845 |
| rs372786040 | snp | C/G | 1.70939e-05 | 0.00292346 | utr-variant-5-prime, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576646 | CCATAACGACCAGAA[C/G]ACGCTGCAGCCACTA | 146845 |
| rs372815043 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9622767 | CTCAGTGACTTATCA[C/T]ACCTATATGACTACC | 146845 |
| rs372834641 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9578783 | ATTCCTGACCTCAGG[C/T]GATCCACCCGCCTTG | 146845 |
| rs372837937 | snp | C/T | 0.000190185 | 0.00974968 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633065 | TTTGAAAAAATAACG[C/T]TCTGTTTAGAACAAC | 146845 |
| rs372844877 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | CFAP52 | GRCh38.p7 | 17:9634529 | GTTGGAGGTTGCAGT[G/T]AGCCGAGACCACGCC | 146845 |
| rs372859730 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9599081 | TTATATATTCAGGTT[G/T]CATATTCCTTATCTG | 146845 |
| rs372877907 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9591599 | AATTTGTGTTTGTGC[A/G]GGGTGCAGTGGCTTA | 146845 |
| rs372924224 | snp | C/T | 3.29962e-05 | 0.00406165 | intron-variant | CFAP52 | GRCh38.p7 | 17:9628825 | CATCATTTCAGGTAA[C/T]GTCCACATGTCAAGA | 146845 |
| rs372928293 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9616147 | GTGTGTGCGCGCACC[A/G]TGCGCGAGCCGAAGC | 146845 |
| rs372943646 | snp | A/G | 1.69899e-05 | 0.00291456 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632846 | GTGGAGAGAGGGTGC[A/G]TATACTGATCCTGCC | 146845 |
| rs373056043 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9623447 | CTTTCATATGTTTGT[A/G]TTAAATCTTTATACA | 146845 |
| rs373060894 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9637989 | GGGTCTTGGGAGGGA[C/T]TTCTTACCATATGCA | 146845 |
| rs373202360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9634576 | GCCTGGGTGACAGAG[C/T]GACATTTTGTCTCAA | 146845 |
| rs373249031 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9595040 | GGATTACAGGTGCCC[A/G]CCAACACACCCGGCT | 146845 |
| rs373296174 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9613905 | GTTATTTCTAACAGT[G/T]AAAATGGCTGCTGCT | 146845 |
| rs373405681 | snp | C/G/T | 0.000103951 | 0.00720873 | utr-variant-3-prime, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643226 | GTCTCTGAGCCTTGG[C/G/T]GTTGCACGCAGTCCT | 146845 |
| rs373408939 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9602459 | GGACATGAACTCATT[C/G]TTTTTTATGGCTGCA | 146845 |
| rs373430345 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9596872 | AGGTGCCCACCACCA[C/T]GCCTGGCTAATTTTT | 146845 |
| rs373475045 | snp | G/T | | | upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576085 | CAGGAAGGTGGGAGC[G/T]CTGCAAGACCTCTCT | 146845 |
| rs373499244 | snp | C/T | 0.000148401 | 0.00861269 | intron-variant, synonymous-codon | CFAP52 | GRCh38.p7 | 17:9585945 | AGAGTACATCGCCTC[C/T]GGACAAGTCACATTC | 146845 |
| rs373511228 | snp | A/C/T | 0.000251878 | 0.01122 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638747 | ATGAGATCTTTCCAG[A/C/T]GCAAGAGAAAAGCAG | 146845 |
| rs373515583 | in-del | -/TTTTT/TTTTTTT/TTTTTTTTT | 0.0667028 | 0.170006 | intron-variant | CFAP52 | GRCh38.p7 | 17:9589801 | CATTCTTAGCTCAAC[-/TTTTT/TTTTTTT/TTTTTTTTT]TTTTTTTTTTTTTTG | 146845 |
| rs373522355 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9622222 | AGATTCTTTTTGTTT[C/T]GGAATTCTTTCAGAA | 146845 |
| rs373688210 | in-del | ATT/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9640442 | GTGTTGTTTCCCCAC[ATT/G]TGTCCATCTCTTTTC | 146845 |
| rs373711395 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CFAP52 | GRCh38.p7 | 17:9628567 | CAGGTTTGAGCCACC[A/G]CGCCCAGCCTTTTCC | 146845 |
| rs373719149 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9589590 | ATACAAAAATTAGCC[A/G]GGCATGGTGGCAGGC | 146845 |
| rs373773741 | in-del | -/C | 0.0123036 | 0.0774623 | intron-variant | CFAP52 | GRCh38.p7 | 17:9636174 | AGTGAAACTCTGTCT[-/C]AAAAAAAAGAAAGAA | 146845 |
| rs373812552 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CFAP52 | GRCh38.p7 | 17:9630626 | TAGTAGAGACGGGGT[G/T]TCACCGTGTTAGCCA | 146845 |
| rs373824609 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9607907 | AGAACCTTCATGAAC[A/G]TCCTCCAGGCAATGT | 146845 |
| rs373863694 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9639735 | AGCTCCTTCAGCTGG[A/G]GTGGTGGGTGAAGGC | 146845 |
| rs373880904 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9579729 | TCCACCACCACGCCT[A/G]GCTAATTTTTGTATT | 146845 |
| rs373886434 | snp | A/G | 8.29401e-05 | 0.00643919 | intron-variant | CFAP52 | GRCh38.p7 | 17:9594338 | TATGTGTCTGCGTTC[A/G]GAGTTTTCAGAACTC | 146845 |
| rs373942220 | snp | A/G | 0.000153988 | 0.00877328 | splice-donor-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641836 | TGCACTTTGTCACAG[A/G]TTAGTCCTGGGATAG | 146845 |
| rs373943166 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584320 | GGAGTACGGGAGTTG[C/T]CTGTGGAAAGAGGTG | 146845 |
| rs373993142 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585046 | TTTATATTTACCCAA[A/C]CTTTGCCTGAGGTAG | 146845 |
| rs374020468 | snp | A/G | 6.58989e-05 | 0.00573978 | missense | CFAP52 | GRCh38.p7 | 17:9612362 | TTCGAGGAGAAGGAC[A/G]CCAGTTTCTCGTAGG | 146845 |
| rs374035006 | snp | C/T | 1.65037e-05 | 0.00287256 | stop-gained | CFAP52 | GRCh38.p7 | 17:9632908 | AACGACGGTAAAATC[C/T]GAGCCTTCGCCCCAG | 146845 |
| rs374075070 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CFAP52 | GRCh38.p7 | 17:9581011 | CCCAAATATCCATTG[A/G]TAAGAAGTTTTAAAA | 146845 |
| rs374124867 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9634074 | ATGATCATGCTCAAC[A/T]TTTTCTTCCCATTAT | 146845 |
| rs374139528 | snp | A/G | 0.000795927 | 0.0199331 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585990 | GAATACAGTGAAAAC[A/G]ACTCATTGTCAATTT | 146845 |
| rs374150822 | snp | C/T | 9.90606e-05 | 0.00703708 | intron-variant | CFAP52 | GRCh38.p7 | 17:9635354 | GAATCTTTTCCTATC[C/T]CTTCAGAAGTCCCAA | 146845 |
| rs374181446 | snp | A/G | | | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9574772 | CTCCCGACCTCAGGT[A/G]ATCTGCCTGCCTCGG | 146845 |
| rs374232029 | in-del | -/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9607464 | TCAAGCCTTTTTTTT[-/T]CTTTGGAGAGAATGG | 146845 |
| rs374237010 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9627580 | TTTATTCTCTCTTAA[C/T]ACAAGCAATCCAAGG | 146845 |
| rs374255574 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9620033 | AAGGAAATAAAGGGT[A/T]TTCAATTAGGAAAAG | 146845 |
| rs374319427 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9619618 | TAAAATACTGGCAAA[A/C]CGAATCCAGCAGCAC | 146845 |
| rs374339508 | snp | A/G | 0.000181271 | 0.00951855 | missense | CFAP52 | GRCh38.p7 | 17:9628787 | ACCTGCCACGGCATC[A/G]ACTTCATGAGGGACG | 146845 |
| rs374357992 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9630049 | GAGTCCTCACTGCCT[C/T]CCCTTTTTCTCTTAT | 146845 |
| rs374415605 | snp | C/G | 1.6684e-05 | 0.00288821 | intron-variant | CFAP52 | GRCh38.p7 | 17:9612521 | TGGAGATTTGATGCA[C/G]TGTGCCAGGGCATTT | 146845 |
| rs374417617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9613890 | ATTAGGTCTTTCCAC[A/G]TTATTTCTAACAGTG | 146845 |
| rs374452873 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641910 | ACTCCCAGGCTAGAG[A/G]CAATTGGAAAAGACA | 146845 |
| rs374465034 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9590543 | TTCAACTTAAAGCAG[C/T]TATTCTCAACCTTTG | 146845 |
| rs374580976 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9627909 | TATATTTTTATTTTT[G/T]GGGGAGGCAGGGTCT | 146845 |
| rs374591347 | in-del | -/A | | | upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576499 | ATAGCACAAAAAAAA[-/A]GAAGAGGAGTCCCAC | 146845 |
| rs374603537 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9589319 | TGTATAGTTATATAA[C/T]GATAGTTCTTCTCTT | 146845 |
| rs374613731 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9585407 | GGCGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 146845 |
| rs374636239 | in-del | -/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9586586 | AAAAAAAAAAAAAAA[-/G]AAAGAAAAAAGAAAA | 146845 |
| rs374648753 | snp | A/G | 1.68235e-05 | 0.00290026 | missense | CFAP52 | GRCh38.p7 | 17:9628674 | GGCTTCCTTGCAGTG[A/G]CACTGCTGAGCTATT | 146845 |
| rs374683747 | snp | A/C/T | 0.00034981 | 0.0132208 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600020 | TGCTGATATTACAGG[A/C/T]GTGAGCCACCGAGGC | 146845 |
| rs374711328 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9602817 | GCCATTCTAACTAAC[A/G]TGAGATGGTATCGCA | 146845 |
| rs374713837 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9604389 | ACCTGAATAAGGACT[A/G]TTACCCAAAATATAC | 146845 |
| rs374717115 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9632481 | AATAAGTGGTTGTAA[A/G]CAAGAGTGGAAGCAA | 146845 |
| rs374719934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585551 | TGGCGGGTGCCTGTA[A/G]TCCCAGCTACTCGGG | 146845 |
| rs374743540 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9625454 | ATAATTTAGCTACCC[A/C]ACAGAGATTTGTGCA | 146845 |
| rs374779993 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9579109 | GGCAGCGTGGGGATT[A/G]GGGAGCTTATGATTT | 146845 |
| rs374787564 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9629052 | CATTGCTGCATATAG[C/T]GTGAATCTTTCTCTC | 146845 |
| rs374814307 | in-del | -/AA/AAAAAA/AG | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631082 | AAGAAAGAAAGAAAG[-/AA/AAAAAA/AG]AGAAAGAAAGAAAGA | 146845 |
| rs374891427 | snp | A/C/T | 0.000704497 | 0.018756 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643005 | CAGCAATGCCATATA[A/C/T]GTGTTTATCTTTTTC | 146845 |
| rs374893195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9578306 | CAGGACATGACGGCA[C/T]GTTAAGTGGGAAGCC | 146845 |
| rs374896694 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9600241 | TCACTGGCAGCATGT[A/G]CTTTTTTTTTTCCTT | 146845 |
| rs374954451 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9611171 | TGCACAAGAACCTGC[A/G]TTGAATTCTTCATTG | 146845 |
| rs374966471 | snp | C/G/T | 3.2955e-05 | 0.00405914 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600199 | GTGAGTAGAGACCAT[C/G/T]GCCACTGCCCTGCCA | 146845 |
| rs375006633 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9587223 | TTTATGGCTGCGTAG[C/T]AGTCCATGATGTATA | 146845 |
| rs375017084 | snp | C/T | 1.70933e-05 | 0.00292341 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641689 | ATGACTCTCCTGAGC[C/T]GAGTCCTGCTTAATG | 146845 |
| rs375042493 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CFAP52 | GRCh38.p7 | 17:9634533 | GAGGTTGCAGTGAGC[C/T]GAGACCACGCCATTG | 146845 |
| rs375072760 | snp | A/C/G | 1.70287e-05 | 0.00291788 | intron-variant | CFAP52 | GRCh38.p7 | 17:9608104 | GCTTTTTCTTAACAC[A/C/G]GTTTTTCCCCCTAGG | 146845 |
| rs375080248 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9633407 | ATGGGGTTTCACCAT[A/G]TTGGCCAGGCTGGTC | 146845 |
| rs375084136 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9613122 | CCCATCTTAAGACAC[A/G]AAGTATCTGTGGTAC | 146845 |
| rs375135798 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9609049 | AGGGATGGGCTTAAA[C/T]AAAAACCAGATACCC | 146845 |
| rs375189527 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9635738 | GATGCTAGTGGGGAG[C/G]GTTACAATTTCCAGG | 146845 |
| rs375202664 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9614021 | AGTAGAATTAATCTG[C/T]AAAACTGTTTGGCCC | 146845 |
| rs375204740 | snp | C/G | 1.66971e-05 | 0.00288934 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586013 | GTCAATTTATCTAGA[C/G]GTGCCTCCCTAGAAG | 146845 |
| rs375210133 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9598886 | GCTGTCATCAAACAC[C/T]GAAAGCCTGCCTCAC | 146845 |
| rs375254472 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9604798 | AAATAAATAAATAAA[A/T]AAATAAAAGAAGATA | 146845 |
| rs375285694 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9596044 | ATGTATATGTATGTA[G/T]ATATATATGTGTGTG | 146845 |
| rs375298362 | snp | C/G/T | | | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575648 | CGGGATGTGGCTGAG[C/G/T]CCCCTCAGTAAAGGA | 146845 |
| rs375306919 | snp | A/T | 3.43124e-05 | 0.00414186 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598202 | ATGGGTGTCCATTTG[A/T]TTGTGGTTTTTTGTT | 146845 |
| rs375375563 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9584394 | CTCAGAACTGAAACC[A/G]AAAGTTAAAAAAATT | 146845 |
| rs375398495 | in-del | -/TTTA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9632719 | ATGGGTGGTGGCAAC[-/TTTA]CTGTAGAAGGGAAAG | 146845 |
| rs375400825 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631133 | GAATTTGCCATATTT[A/T]GGGCTCAAAAGTCTT | 146845 |
| rs375455925 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9613906 | TTATTTCTAACAGTG[A/G]AAATGGCTGCTGCTT | 146845 |
| rs375470115 | in-del | A/GG | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9591226 | ATTTTTAGTAGAGAC[A/GG]GGGTCTCTTCATGTT | 146845 |
| rs375495892 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600442 | CAGACAGGGTTTCAT[C/G]ATGTTGGCTAGGCTA | 146845 |
| rs375565819 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | CFAP52 | GRCh38.p7 | 17:9578826 | GCTGGGATTACAGGC[G/T]TGAGCCACCACACCC | 146845 |
| rs375601157 | in-del | -/TT/TTT | 0.0984431 | 0.198823 | intron-variant | CFAP52 | GRCh38.p7 | 17:9588774 | AGCCACAGAAAAGAA[-/TT/TTT]TTTTTTTTTTTTTTT | 146845 |
| rs375627253 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9641246 | GAGCAGAAGGGAAAG[C/T]TGGGAATAAGGGTGG | 146845 |
| rs375629381 | in-del | -/TTC | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9629496 | TCTTTCTTTCTTTCT[-/TTC]TTTCTTTTCTTTCTT | 146845 |
| rs375635877 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CFAP52 | GRCh38.p7 | 17:9630775 | GGTTTCGCCTGAGGT[C/T]AGGAGTTTGAGAACA | 146845 |
| rs375643778 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9591988 | AAAGCATGACTCTTA[C/T]ATCCCCCTCACCTTG | 146845 |
| rs375706369 | snp | A/G | 0.000163987 | 0.00905353 | missense, upstream-variant-2KB, utr-variant-5-prime | CFAP52, STX8 | GRCh38.p7 | 17:9576744 | GCGGAGCTGGAACTT[A/G]ACGCCGTGATCGGCT | 146845 |
| rs375721567 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9632488 | GGTTGTAAGCAAGAG[C/T]GGAAGCAAGCATAAG | 146845 |
| rs375725968 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9595627 | GCAACATTTCTTCAG[A/G]ACTCAATACTTGAAT | 146845 |
| rs375795363 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9622374 | CAAGATGGTGAGACA[A/C/G]CCCTTCCTCATCTTT | 146845 |
| rs375819790 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9613707 | TATTTTTGGTAGAGA[C/T]GGGGTTTCACCTTGT | 146845 |
| rs375846701 | snp | A/G | | | upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576556 | CCTTCATTTCCAAGA[A/G]TGCTAATGAACTCGA | 146845 |
| rs375859241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9623044 | CATTTACTGAGAAAA[A/G]TGTTAAGGTCTCAGG | 146845 |
| rs375890438 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9638240 | CACTTCCAAATGGTG[A/G]CCTCAGGACTCAAGT | 146845 |
| rs375905449 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642932 | GACAGATACATGGGG[A/G]CCATGTTGAAAATGA | 146845 |
| rs375991904 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9627628 | AATGTTATAGGTGTC[A/G]ACTTATCTTCAAACT | 146845 |
| rs376052876 | in-del | -/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9607464 | GTCAAGCCTTTTTTT[-/T]CTTTGGAGAGAATGG | 146845 |
| rs376092927 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9607562 | ATGTTGTAGTTCAGA[C/T]AATACAGTCGCCAAA | 146845 |
| rs376104539 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576920 | GAGGACCCGCACAGC[C/G]TGACCTGCCCCAAGG | 146845 |
| rs376111874 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9615628 | CTTGAATTGTTTTTT[C/T]TTCTTTTAGGACATA | 146845 |
| rs376170198 | snp | A/T | 4.94588e-05 | 0.00497262 | intron-variant, missense | CFAP52 | GRCh38.p7 | 17:9585937 | AGGTCTGGAGAGTAC[A/T]TCGCCTCCGGACAAG | 146845 |
| rs376192510 | snp | A/C/G/T | 3.30498e-05 | 0.00406497 | synonymous-codon, missense | CFAP52 | GRCh38.p7 | 17:9586733 | TTATAAGAACAGAGA[A/C/G/T]CTGCTTGCTCGGCTG | 146845 |
| rs376197126 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9602396 | TTTCTGTTCCTGTTT[A/T]AGTTTGCTGAGAATG | 146845 |
| rs376215212 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9616192 | CCTCACCTGGGAAGC[A/G]CAAGGGGTCAGGGAG | 146845 |
| rs376220632 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9615681 | CTAGAGCACAGTGAC[A/G]CAATCACAGCTCAGA | 146845 |
| rs376223932 | snp | A/G | 1.66771e-05 | 0.00288761 | missense, upstream-variant-2KB, utr-variant-5-prime | CFAP52, STX8 | GRCh38.p7 | 17:9576699 | AACCTCCCAAGGATG[A/G]ATAACAAAATTTCGC | 146845 |
| rs376260961 | snp | C/T | 3.29554e-05 | 0.00405914 | missense | CFAP52 | GRCh38.p7 | 17:9612413 | ATCGTGTCAGCTTCA[C/T]GGATTTCAAAGAGAC | 146845 |
| rs376283850 | snp | C/G/T | 0.000115758 | 0.00760702 | missense, synonymous-codon | CFAP52 | GRCh38.p7 | 17:9632895 | CATGCCAGCATGGAA[C/G/T]GACGGTAAAATCCGA | 146845 |
| rs376343886 | snp | A/G | 0.000510544 | 0.0159691 | intron-variant, synonymous-codon | CFAP52 | GRCh38.p7 | 17:9585840 | TCCTCTTGGTTGCAC[A/G]GTCCTCATTCAGGCA | 146845 |
| rs376351044 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9609249 | AAGATGAAAAAAAAA[A/T]TCCCTGTCCTCATGG | 146845 |
| rs376352644 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9640395 | TGCTCTTCCTCCCCC[C/G]ACCCACCACCCCCCG | 146845 |
| rs376365503 | snp | A/G | 6.62482e-05 | 0.00575497 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585981 | GTTCAAGGTGAATAC[A/G]GTGAAAACGACTCAT | 146845 |
| rs376365674 | snp | A/G | 0.000101008 | 0.00710591 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638748 | TGAGATCTTTCCAGC[A/G]CAAGAGAAAAGCAGT | 146845 |
| rs376424087 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | CFAP52 | GRCh38.p7 | 17:9636179 | AACTCTGTCTCAAAA[A/G]AAAGAAAGAAAGAAA | 146845 |
| rs376487614 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9640397 | CTCTTCCTCCCCCCA[A/C]CCACCACCCCCCGAC | 146845 |
| rs376608849 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9640948 | TGCACCCAGCTGGCC[A/G]TATCGCATTTTCTTT | 146845 |
| rs376618267 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9594010 | AACTTTTAATGTGTC[A/G]CCGTTGTGTCTTCTA | 146845 |
| rs376630630 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631452 | TTTTAAACTGCTAAG[A/G]TCAAGAGGTGACATT | 146845 |
| rs376634882 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9609781 | GATTGGGCTTATTGA[A/G]AATGTTTTAGACCAG | 146845 |
| rs376641266 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9593662 | GTTTTCACCATGTTG[A/G]CCAGGTTGGTCTCAA | 146845 |
| rs376661862 | snp | C/T | 1.64917e-05 | 0.00287151 | missense | CFAP52 | GRCh38.p7 | 17:9612314 | CTCCCTAAAGGAAGA[C/T]TCAGTTACAAGGCGG | 146845 |
| rs376690628 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9639212 | AGGCGGGTGGATCAC[C/T]TGAGGTCAGGAGTTC | 146845 |
| rs376743248 | snp | A/G | 1.6489e-05 | 0.00287128 | synonymous-codon, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641819 | TATCACACAGGAAGG[A/G]GTGCACTTTGTCACA | 146845 |
| rs376777837 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9591324 | ATTATAGGCTTGAGT[C/T]GCCGCTCCCGGCCTG | 146845 |
| rs376782068 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9623753 | TCAAGTGTCCATTCA[C/G]CCGCATGATCATAGC | 146845 |
| rs376821054 | snp | C/T | 3.33122e-05 | 0.00408105 | intron-variant | CFAP52 | GRCh38.p7 | 17:9594359 | TTCAGAACTCATAAA[C/T]TGCTATATTTTCTTG | 146845 |
| rs376871396 | in-del | -/AA | 0 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9589745 | CTCAAAAAAAAAAAA[-/AA]TAAATAAAGAAAAGA | 146845 |
| rs376933591 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9620107 | TCTAGAAAACCCCAT[C/T]GTCTCAGCCCAAAAT | 146845 |
| rs376962992 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | CFAP52 | GRCh38.p7 | 17:9594016 | TAATGTGTCACCGTT[A/G]TGTCTTCTAATACCT | 146845 |
| rs376992708 | in-del | -/AAAC | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9610214 | AAGTAAAAAACAAAC[-/AAAC]TATGTTGGGTTATCT | 146845 |
| rs377029555 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B | CFAP52, USP43 | GRCh38.p7 | 17:9643427 | ACTTTTAACATTTTG[A/G]ATAAATTCTTAGTTG | 146845 |
| rs377115961 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | CFAP52 | GRCh38.p7 | 17:9628827 | TCATTTCAGGTAACG[C/T]CCACATGTCAAGATC | 146845 |
| rs377246653 | snp | C/G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9630554 | CCTGCCTCAGCCTCC[C/G/T]GAGTAGCTGGGACTA | 146845 |
| rs377300892 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9579509 | AAACAAATTAGAAAC[A/G/T]AAAGCAAGGCCCCTT | 146845 |
| rs377327479 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9629609 | CTGGAGTGCAATGGC[A/G]CGATCTAGGCTCACT | 146845 |
| rs377330350 | snp | A/G | 1.66192e-05 | 0.00288259 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585998 | TGAAAACGACTCATT[A/G]TCAATTTATCTAGAG | 146845 |
| rs377355973 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9640613 | GTATTCCGTGGTATA[A/T]ATCTGCCACATTTTC | 146845 |
| rs377374357 | in-del | -/TTTG | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9613503 | TGTTTTTGGGGGGTT[-/TTTG]TTTGTTTGTTTGTTT | 146845 |
| rs377388823 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9607246 | AGCTACTCTGGTGGG[C/T]GAGTCACAAGAATCG | 146845 |
| rs377393859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9639713 | ATGATACTGGCGGGC[A/G]GGGGAAAGCTCCTTC | 146845 |
| rs377505636 | snp | A/G | 0.000323154 | 0.0127072 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598373 | TAACAATTAGCACAC[A/G]TTCCTGTTAGCAGTG | 146845 |
| rs377565869 | snp | A/G | 4.94271e-05 | 0.00497102 | missense | CFAP52 | GRCh38.p7 | 17:9612373 | GGACACCAGTTTCTC[A/G]TAGGAACAGAAGAAT | 146845 |
| rs377620912 | in-del | -/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9641417 | GTGGATGCAGAGGCT[-/G]GTTCTTTCTTTTACA | 146845 |
| rs377657255 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585596 | GAATCACTTGAACCC[A/G]GGAGGTGAAGGTTGC | 146845 |
| rs377695807 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9579754 | TGTATTTTTAATAGA[C/G]ACGGTGTTTCGCCAC | 146845 |
| rs377696038 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9602552 | TTGGGTTGGTTCCAA[A/G]TCTTTGCTATTGTGA | 146845 |
| rs377764878 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9603455 | ACCCCGTGATCCACC[C/G/T]GCCTCGGCCTCCCAA | 146845 |
| rs386385628 | in-del | -/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9603154 | TGCTGGCTATCTTAG[-/G]GTTTCTCAAACCTTT | 146845 |
| rs386385629 | in-del | -/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9603155 | GCTGGCTATCTTAGG[-/G]TTTCTCAAACCTTTG | 146845 |
| rs386795205 | multinucleotide-polymorphism | CT/TA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9581416 | ATAGATGTATATAAA[CT/TA]AATGAGGAAAGATGT | 146845 |
| rs386795206 | multinucleotide-polymorphism | AGA/GGC | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9584375 | TCAGAGCACCTGGTG[AGA/GGC]ACTCAGAACTGAAAC | 146845 |
| rs386795207 | multinucleotide-polymorphism | AC/GT | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9585442 | GGGAGGCTAAGGTGG[AC/GT]GGATCACGAGGTCAG | 146845 |
| rs386795208 | multinucleotide-polymorphism | ATG/GTC | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9593826 | AAGAATTACCCGGAC[ATG/GTC]GTGGTGTGCGTCTGT | 146845 |
| rs386795209 | in-del | AT/GTC | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9624664 | TAATCCAGTACCTGG[AT/GTC]TACTTGGAATCAGTT | 146845 |
| rs386795210 | in-del | CTTTCTTTTC/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9629491 | TTTCTTTCTTTCTTT[CTTTCTTTTC/T]TTTTCTTTCTTTCTT | 146845 |
| rs386795211 | multinucleotide-polymorphism | GT/TG | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9632253 | AGGCAAGTTTTTTTT[GT/TG]TTTTTTTTTTTCATA | 146845 |
| rs386795212 | in-del | CG/TCA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9632265 | TTTTGTTTTTTTTTT[CG/TCA]TATTTTTTGTAGAGA | 146845 |
| rs386795213 | multinucleotide-polymorphism | CG/TA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9633659 | AGGATCGTGGTTGTA[CG/TA]AATTGTCATCTTATC | 146845 |
| rs386795214 | in-del | AC/GCA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9637071 | CAAACAAACAAAAAA[AC/GCA]AAAAAAAACCCGACA | 146845 |
| rs397697920 | in-del | -/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9598227 | TTGTTTTTTTTTTTT[-/T]ACATAGTGGGACAAT | 146845 |
| rs397702945 | in-del | -/AC | 0 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9606403 | CACACACACACACAC[-/AC]GAACATGCAAATACA | 146845 |
| rs397750152 | in-del | -/TT/TTG/TTTG | 0 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9594910 | TTTTTTTTTTTTTTT[-/TT/TTG/TTTG]GACAGTGTTTTGCTG | 146845 |
| rs397759228 | in-del | -/A | 0 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9580335 | AAAAAAAAAAAAAAA[-/A]GCCAGACCCTGTAAA | 146845 |
| rs397778588 | in-del | -/T | 0 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9613904 | GTTATTTCTAACAGT[-/T]GAAAATGGCTGCTGC | 146845 |
| rs397798055 | in-del | -/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9587017 | CTGATCCTCTCCCTC[-/C]TCCCACCCTCCACCC | 146845 |
| rs397857328 | in-del | -/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9611256 | TATACTTTTTTTTTT[-/T]AAGTTCATACTCATT | 146845 |
| rs397950168 | in-del | -/A | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9580767 | AAAAAGAAAAAAAAA[-/A]GGGTAATATAATAAG | 146845 |
| rs397959225 | in-del | -/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9610543 | CCATTTTTTTTTTTT[-/T]GTTTGTTTTGAGATG | 146845 |
| rs398030316 | in-del | -/AAAAA | 0 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9605719 | AAAAAAAAAAAAAAA[-/AAAAA]TCAGTGCTTGCCATG | 146845 |
| rs398030317 | in-del | -/T | 0 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9614174 | TTTTTTTTTTTTTTT[-/T]GAGACTGAGTCTCGC | 146845 |
| rs398078878 | in-del | -/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9611255 | ATATACTTTTTTTTT[-/T]TAAGTTCATACTCAT | 146845 |
| rs527236915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586899 | ATTTCAGGTTCAGAC[A/G]TACATGTGCAGGTTT | 146845 |
| rs527261435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9601528 | GCCATACATAAGAGA[A/G]GTGTGCTCTTTGATC | 146845 |
| rs527301869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9637612 | GTTTAAAATGCAGAT[C/T]CTGGCCAGGCGTGCT | 146845 |
| rs527322603 | snp | A/C/G/T | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585495 | AACATGGTGAAACCC[A/C/G/T]GTCTCTACTAAAAAT | 146845 |
| rs527331548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9594430 | TTAGTCCTGGATAAA[C/T]ACCTTACATCATAGT | 146845 |
| rs527353160 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9604544 | AGGCTGAGGCGGGCC[C/G]ATCACCTGAGGTCAG | 146845 |
| rs527428095 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB, intron-variant | CFAP52, USP43 | GRCh38.p7 | 17:9643720 | TGAGAATTAAGTGAC[G/T]AATGTACTAAAGCAT | 146845 |
| rs527488894 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633174 | TGATGAGATCTGAAA[A/C]TATGTCATAAATAAA | 146845 |
| rs527515278 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584681 | GGCTGGAGTGCAATA[G/T]TGTGATCTCGGCTCA | 146845 |
| rs527633426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632704 | TGGCTTAGGCAACTG[A/G]ATGGGTGGTGGCAAC | 146845 |
| rs527649320 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9625117 | TACTTAAAAAGGCAA[A/G]CAAACAAAAAAGCAA | 146845 |
| rs527655863 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9587057 | CCCAGTGTCTGTGTT[C/G]CCTTCTATGTGTTCA | 146845 |
| rs527717707 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9582163 | CTCTGGGCAGGTTGC[A/T]CACCTAAGAATAGAG | 146845 |
| rs527758479 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9591889 | TCTCAAAAAAAAAAT[G/T]GTTTTTGAAAAATTA | 146845 |
| rs527763401 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9627095 | CATTGGTAATTTACA[C/T]TGTATTTAGAGGTTG | 146845 |
| rs527792383 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600403 | TGCCCCACCACACCC[A/G]ACTAATTTTTGTATT | 146845 |
| rs527794501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586423 | ACAAAATTAGCAGGG[C/T]GTGCTGGTGCATGCC | 146845 |
| rs527824564 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9636931 | GTGCCTGTTATCCCA[A/G]CTACTCAGGAGGCTG | 146845 |
| rs527831136 | snp | A/G | 0.238749 | 0.249747 | intron-variant | CFAP52 | GRCh38.p7 | 17:9631064 | AGAGAGAAAGAAAGA[A/G]AGAAAGAAAGAAAGA | 146845 |
| rs527881203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9606595 | CTGGCTTGCAAGTAA[C/T]AGAGCTGAGATTTCA | 146845 |
| rs527883783 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9614307 | ACTACAGGCATGTGC[C/G]ACCGCGCCCAGCTAA | 146845 |
| rs527914847 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9597438 | AGCTTGATTTTGCTA[G/T]TCTACAATGTGTATA | 146845 |
| rs527924255 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9594986 | ACCTCCACCTCCCGG[A/G]TTCAAGCAATTCTCC | 146845 |
| rs528024662 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9626283 | TGCCCAGGCTGGAGT[A/G]TAATGGCATGATCTC | 146845 |
| rs528056451 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9640183 | GAGAAACAAATGAAA[C/T]GCACGTGCAGGTTTG | 146845 |
| rs528061673 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9574762 | TGGTCTCGACCTCCC[A/G]ACCTCAGGTGATCTG | 146845 |
| rs528088239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9612015 | GTCATTTGTACCCAT[A/G]TGCCTGCCTGGAATA | 146845 |
| rs528144748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9622984 | ATGTAGTTAGTGTCA[C/T]ACAGATCTTCTTCTC | 146845 |
| rs528146657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9630133 | TCACCCCTCATTATC[C/T]TCCCCCTTATCCTAG | 146845 |
| rs528154198 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9605249 | CATCCAAACAATGGC[A/G]TATTAATCAGTACTA | 146845 |
| rs528166739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9580884 | ATTCTTAATGAAGAT[A/G]ATCTTTGAGCTTTTA | 146845 |
| rs528207377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9623596 | TGACTATTTCTGATG[A/G]TCTTCATTCTTTCTT | 146845 |
| rs528278207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9599993 | TGATCCACCCGCCTC[A/G]GCCTCCCAAAGTGCT | 146845 |
| rs528289394 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642440 | ACCAGCCTGGCCAAC[A/C]TGGTGAAACCCTGTG | 146845 |
| rs528312333 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9607551 | TTATGTAGTACATGT[G/T]GTAGTTCAGATAATA | 146845 |
| rs528339503 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | CFAP52 | GRCh38.p7 | 17:9592494 | AAAAAATAAAAAGAA[A/C]CCCCGTACCCATTAG | 146845 |
| rs528349561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9605146 | GAACCTGCACACAGA[C/T]GTTTACAGAAGCTTT | 146845 |
| rs528387725 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9582647 | GTAATTAAATTTTTT[G/T]ATTTTTTGAGAAAGA | 146845 |
| rs528399580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9605779 | GGGTAAAGCACAGAG[A/G]ATGTTTTGGGCAGTG | 146845 |
| rs528413971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9599258 | GCACTCAACAATTTC[C/T]GATTTTGGAGCATTT | 146845 |
| rs528461216 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9604291 | GGACTTCCTTAAAAT[A/C]AAAAATTCTGCTCCA | 146845 |
| rs528492179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9640524 | TCCTGCGTTAGTTTG[C/T]TGAGGATAATGGCTC | 146845 |
| rs528545280 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9610540 | TTCCCCATTTTTTTT[G/T]TTTGTTTGTTTTGAG | 146845 |
| rs528606180 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9603613 | TCCCAATAAACATCC[C/G]AGCAAGTTATTTTGT | 146845 |
| rs528715729 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CFAP52 | GRCh38.p7 | 17:9580415 | ATTAAAGTTCATGTG[C/T]GGTGGCTCACACCTG | 146845 |
| rs528768347 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9591076 | GAGTTTCACTCTTGT[G/T]TCCCAGGCTGGAGTG | 146845 |
| rs528822124 | snp | C/T | 1.64882e-05 | 0.00287121 | intron-variant | CFAP52 | GRCh38.p7 | 17:9635386 | TGTGGATCAAGATCC[C/T]GTGCTCTGTGGCTTT | 146845 |
| rs528836025 | in-del | -/ATG | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9577305 | AAGGAAGGTTTCTAA[-/ATG]ATGAGGATTTCAGAC | 146845 |
| rs528897677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9606378 | GCAGAGACCCTGTCT[C/T]CAAAATACACACACA | 146845 |
| rs528924142 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600010 | CCTCCCAAAGTGCTG[A/G]TATTACAGGCGTGAG | 146845 |
| rs528937581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9624457 | TTGAGTCCACCTAGT[A/G]AATTTATTTTAGTTA | 146845 |
| rs528958203 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575682 | GTCTCGCTGCCCCTC[C/T]CCTCATCCCGAAAGG | 146845 |
| rs529150691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9587219 | CTTTTTTATGGCTGC[A/G]TAGTAGTCCATGATG | 146845 |
| rs529164691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632171 | CAACCTCCATCTCCC[A/G]GGTTTAAGTGATCCT | 146845 |
| rs529295291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9591568 | GTTGCCCTTTGTTTT[A/G]TCTATTTTTAAAACA | 146845 |
| rs529297532 | snp | A/C | 1.64746e-05 | 0.00287002 | intron-variant, missense | CFAP52 | GRCh38.p7 | 17:9585876 | TACTAAAGAGCAGAA[A/C]TTCCTACAGGGTCAT | 146845 |
| rs529312868 | snp | A/C | 1.64738e-05 | 0.00286995 | missense | CFAP52 | GRCh38.p7 | 17:9635448 | CCCAGAAGCTGGAGG[A/C]GGCCCTGAAGGAACA | 146845 |
| rs529313316 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9635612 | AATCCAATCATGCCA[A/T]CAGTTTATTGAACAT | 146845 |
| rs529314545 | snp | C/T | 9.89707e-05 | 0.00703389 | missense, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641740 | TTGCTTACTGGGAAG[C/T]ATTTGATGGGACAGT | 146845 |
| rs529346630 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9599140 | TTTTGGATTTTCTTC[A/C]GATTTTGGAGTATTT | 146845 |
| rs529347773 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9604406 | TACCCAAAATATACA[C/G]AGAACTTTTAAAACT | 146845 |
| rs529412021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598413 | GTGTTTGTGTGTGTG[C/T]ACATGGGGCTGGGGA | 146845 |
| rs529483330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9623694 | TTTGTTTGTTTGTTT[A/G]TTTGTTTAAGAGACA | 146845 |
| rs529530529 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9574899 | AATAACCTAGATTCC[A/C]GGTAACTCAACTTTG | 146845 |
| rs529552869 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586134 | ATTCCGTCAGACCGG[G/T]AGTGAAGGACTCTGA | 146845 |
| rs529582742 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9635899 | AATGCAAGGTCGGGC[A/G]TGGTGGCTTCTGCCT | 146845 |
| rs529646284 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | CFAP52 | GRCh38.p7 | 17:9616022 | AATAGGAACAGCTCC[-/G]GGTCTACAGCTCCCA | 146845 |
| rs529686765 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585508 | CCCGTCTCTACTAAA[A/T]ATACAAAAAAAAATT | 146845 |
| rs529722820 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633945 | CTCGGCCTCCCAAAG[A/T]GCTGGGATTACAGGC | 146845 |
| rs529781256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9628611 | AACACATTTTGGTGT[C/T]AAATATGCATCTGGG | 146845 |
| rs529823761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585435 | GCACTTTGGGAGGCT[A/G]AGGTGGACGGATCAC | 146845 |
| rs529825623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9590139 | GCTGTGATACGTGTG[A/G]TGATCAATCTTCTTC | 146845 |
| rs529827481 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9634507 | AAAATTAGGCCAGGC[A/G]TGGTGAGTTGGAGGT | 146845 |
| rs529921221 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9614374 | TTGGCCCAGCTGGTC[A/G]CGAGCTCCCAACCTC | 146845 |
| rs530032740 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9608795 | AGCACCTCCTCCAAC[C/G]AAACCAATGTATTAG | 146845 |
| rs530167243 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CFAP52 | GRCh38.p7 | 17:9615756 | CTGGGATGCAGGCAT[G/T]TACCACCATGCCCAG | 146845 |
| rs530179660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9627655 | AACTCAGGTAATATA[C/T]ATTAAATATGTTCAG | 146845 |
| rs530186874 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9591649 | TTGGGAGGCCAAGGC[A/G]GAAAGGATCACTTGA | 146845 |
| rs530189892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9578500 | TGCTTATCTCAAGAT[A/G]AGTGCTTGTTTAGCT | 146845 |
| rs530215330 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | CFAP52 | GRCh38.p7 | 17:9637883 | ACTCGGCCCATAATA[C/T]CCATTTTAAAAATAC | 146845 |
| rs530273217 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9624705 | CTCTGCCTTTTTTTT[C/G]AGTCATATTTTCCTA | 146845 |
| rs530287631 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9609484 | TGGATCGCTTGAGCC[C/G]AGGAGTTCCAGCCCA | 146845 |
| rs530302424 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | CFAP52 | GRCh38.p7 | 17:9596720 | GTTGTGTGTGTGTGT[G/T]TGTTTTTTTTTTGAG | 146845 |
| rs530350690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9595485 | AACTGACCACGGGCT[A/G]TGGCGACACTCTTCA | 146845 |
| rs530366141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9589610 | TGGTGGCAGGCGCCT[A/G]TAATCCCATCTACTC | 146845 |
| rs530468634 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9580210 | TAGCTATGCCCATTT[G/T]TTTATGTATTGTCTA | 146845 |
| rs530515146 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636160 | GCCTGGGCAACAAGA[A/G]TGAAACTCTGTCTCA | 146845 |
| rs530546470 | snp | G/T | 0.0298908 | 0.118541 | intron-variant | CFAP52 | GRCh38.p7 | 17:9629719 | TCAGCCTCCCAAGTA[G/T]CTGGGACTACAGGCG | 146845 |
| rs530588649 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9604700 | TTGAACCCGGCAGTG[A/T]GATCACGCCATTGCA | 146845 |
| rs530627816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9602628 | TCCTTTGAGTATATA[C/T]GCAGTAATGGGATTG | 146845 |
| rs530700795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9605067 | AACTTACTCTTACCA[C/T]GTAATGCAGCAGTTG | 146845 |
| rs530704984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598499 | AGGTGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 146845 |
| rs530728577 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9611993 | AATAAAGGGGTTAGT[G/T]GCTGTGGTCATTTGT | 146845 |
| rs530769480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9599159 | TTTGGAGTATTTGCA[C/T]TATACTTCCAAGTTC | 146845 |
| rs530783487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9611282 | TCATTATAAAGGGAA[A/G]AGGGAGAAATCTGAA | 146845 |
| rs530789027 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9603240 | TTGATACAGAGTCTC[A/G]CTCTGTCGCCCAGGC | 146845 |
| rs530848281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9596803 | TCACTGCAACCTCCA[C/T]CTCCCAGGTACAAGC | 146845 |
| rs530851433 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9603556 | GACTCAGTATTGTCA[C/T]GATATGAGTTCTTCT | 146845 |
| rs530929651 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9609613 | AAGCGGGAGGATTGA[A/T]TGAGGTTGATCAGTC | 146845 |
| rs530990106 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9616294 | CGCTTTTCAGACCGG[C/T]TTAAGAAACGGCGCA | 146845 |
| rs531098011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9639961 | TGAATCCTGAGAAAC[A/G]TGGGTTCTGGCATGG | 146845 |
| rs531099081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9590183 | TTCAGAGCAGGTGGC[A/G]CAGAATCCTCATTCT | 146845 |
| rs531155022 | snp | A/C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585519 | TAAAAATACAAAAAA[A/C/T]AATTAGCCAGGTGTG | 146845 |
| rs531231654 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584163 | TTGGTCATTGTATTT[G/T]CTTTTATTTTTGCTG | 146845 |
| rs531236148 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP52 | GRCh38.p7 | 17:9597663 | CAGAAATTAGCTGGG[C/T]GTGGTGGCGGGCACC | 146845 |
| rs531286756 | snp | G/T | 0.0283406 | 0.115616 | intron-variant | CFAP52 | GRCh38.p7 | 17:9640442 | GTGTTGTTTCCCCAC[G/T]TGTCCATCTCTTTTC | 146845 |
| rs531341523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638943 | AGGATTAAAGTCATG[C/T]TTGCTCATGGTGCTT | 146845 |
| rs531364115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9588962 | ACAAAAATTAGCCAG[A/G]CATAGTGCCGGGGCC | 146845 |
| rs531377480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9578578 | TATTTATTTTGAGAC[A/G]GTGGAGTCTCGCTCT | 146845 |
| rs531439145 | in-del | -/A | 0.0146672 | 0.084371 | upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576491 | CCAGAGAAATAGCAC[-/A]AAAAAAAAGAAGAGG | 146845 |
| rs531440318 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9578865 | GGTGGAGGGGTGCAT[C/G]GCCTTAGGTCCTGTT | 146845 |
| rs531440503 | snp | A/T | | | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642736 | CAATCATATATATGA[A/T]GTATATGTATACCAG | 146845 |
| rs531481836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638343 | TTCTCATTGAGTTTC[A/G]TGCTCTGTCTTTAGG | 146845 |
| rs531482992 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9640664 | TTGGAGACAGAGTCT[C/T]ACTTTGTCACCCAGG | 146845 |
| rs531489664 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584713 | TGCAACCTCCGCCTC[A/G]TGGGTTCCAGTGATT | 146845 |
| rs531577388 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9596067 | TGTGTGTGTATATAT[A/G]TATATATATATATAT | 146845 |
| rs531598567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9626367 | CCCAAGTAGCTGGGA[C/T]TACAGGCGCACACCA | 146845 |
| rs531647764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9577018 | GCCAGCACCTAAAAG[A/G]GACCAAATGCCTCTT | 146845 |
| rs531665429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9637384 | TTCTTGTGCCAAAAT[C/T]TTTAAAAATGCTCAG | 146845 |
| rs531683012 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576317 | ATCAATTATATATAT[A/T]TTTTATAGCAGCCTT | 146845 |
| rs531711295 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631873 | CCCGGGTTCAAGCGA[C/T]TCTCCTGCCTCAGCC | 146845 |
| rs531711420 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9582931 | CATGAGCCACCCAGC[A/C]CAGCCTAGATGTTTT | 146845 |
| rs531720515 | snp | C/T | 0.0821764 | 0.185298 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632088 | TCCACTTTTTTTTTT[C/T]TTTTTTTGAGACAGG | 146845 |
| rs531725428 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CFAP52 | GRCh38.p7 | 17:9605437 | AAAGATCAGGCTGGG[C/T]GCGGTGGCTGACACC | 146845 |
| rs531793571 | in-del | -/A | 0.0402882 | 0.136092 | intron-variant | CFAP52 | GRCh38.p7 | 17:9583279 | CACTCAATTAAAATG[-/A]AAAAAAATCATTTAT | 146845 |
| rs531853925 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9587768 | TGCAAGATACTTTTT[C/T]AGATGCCAAGTTTGC | 146845 |
| rs531861217 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9625574 | TCAACTCTGATCTCT[A/C/G]GCATTGTTAGCTGGT | 146845 |
| rs531866983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9614349 | TTAGTAGAGATGGGA[C/T]TTCACTATGTTGGCC | 146845 |
| rs531980226 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584787 | CCACCAAGCCCAGCT[A/C]ATTTTTTGTATTTTT | 146845 |
| rs531995626 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9600874 | ATTGGCCAGTTCTCT[A/G]TGCCCTCGTCTCTGG | 146845 |
| rs532061345 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9607320 | CACTGCACTCCAGTC[C/T]GAGTGACAGAGAGAG | 146845 |
| rs532067656 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9581254 | CCCGGAAGTGCTGGT[C/T]GCACAGCATTGTGAA | 146845 |
| rs532087796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638991 | ACATAGTAGGTACTC[A/G]ATAGATTGGTTTTTA | 146845 |
| rs532093724 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9609594 | CCAGCTACTCAGGAG[G/T]CTGAAGCGGGAGGAT | 146845 |
| rs532205955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9609864 | TTGGAAGCCTTCCAG[A/G]TTATTATACATGCTC | 146845 |
| rs532219421 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9580072 | TCCTATTATGGTATA[C/G]AAAGAGTTCTTGTAA | 146845 |
| rs532400581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9614916 | TACTGATGCAATTTT[A/G]TAATCAGAGCACTAA | 146845 |
| rs532486380 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9616405 | ATCAAACTGCAAGGC[A/G]GCAACGAGGCTGGGG | 146845 |
| rs532519929 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9577952 | CAAAAATTATCCGGG[A/C]GTGGTGGTAGGTGCC | 146845 |
| rs532637301 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP52 | GRCh38.p7 | 17:9609093 | TATGGCCTCTGCTAC[C/T]CCCAGGAAGCCAGGG | 146845 |
| rs532655199 | snp | C/T | 5.0671e-05 | 0.00503318 | intron-variant | CFAP52 | GRCh38.p7 | 17:9608228 | CCATCAAGTAAGTTC[C/T]GGGTCTCACACAGTG | 146845 |
| rs532674114 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9614467 | GGCCTCTCAAAATAT[G/T]TCTCTTGCCATCAAT | 146845 |
| rs532681203 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9587728 | TTTTGTTTTATCTTA[C/T]AAATTTATTTAAGTT | 146845 |
| rs532792979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9615651 | AGGACATAAGGTCTT[C/T]CTCTGTCACCCAGGC | 146845 |
| rs532796650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9595454 | CGAAAACCAGCCCTA[C/T]CAAGCAACCTAAAGC | 146845 |
| rs532806422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600981 | AGTCATTGGCGGCAC[C/T]ATTCACAATAGCAAA | 146845 |
| rs532816117 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9606013 | GGAAAGAAGTATTGG[C/G]GAAATCTCAAATACT | 146845 |
| rs532843345 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9635818 | TGTCCACACAGTGAA[A/G]CATGGTTTAACTTAC | 146845 |
| rs532855462 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9608748 | TAAAATGAAACAAAA[C/T]CTTATTTATTGCCAT | 146845 |
| rs532877142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9601810 | GTTTCTACTAAACTT[C/T]GAATTTGAAAGCTTG | 146845 |
| rs532917765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9607166 | GCCTGGCCAACATGG[C/T]GAAACCCCATCTCTA | 146845 |
| rs532949059 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP52 | GRCh38.p7 | 17:9587840 | CAAGGGCCCTGTCCC[C/T]TCTAATGTTCTCTCT | 146845 |
| rs532971578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632163 | GCTCACTGCAACCTC[C/T]ATCTCCCAGGTTTAA | 146845 |
| rs533113877 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9635875 | TGAAAGGGGGCAAGA[A/C]AAATAACGAATGCAA | 146845 |
| rs533139007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9592350 | GGTGGGCCCCTGTAA[C/T]CCCAGCTACTAGGGA | 146845 |
| rs533182756 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9588271 | AATTGCCCTGTGGAC[A/G]CTGTGCAGGTGCCCT | 146845 |
| rs533183922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9581160 | TCTCTACTAAAAATA[C/T]CAAAAAATTAGCCGG | 146845 |
| rs533211160 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9604330 | ACTGTCAAGAGAATG[A/C]AAAATAAAGATACAG | 146845 |
| rs533261862 | in-del | -/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9632245 | ACCATGCGAGGCAAG[-/T]TTTTTTTTGTTTTTT | 146845 |
| rs533302964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9582108 | ATGCAAAAACAAAAA[C/T]AAATCTGAAGAAATA | 146845 |
| rs533317760 | snp | A/C | | | upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576593 | CAGGCTGGGTTTCTG[A/C]GCGGGCGTGGAGCTG | 146845 |
| rs533433200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9596352 | GCAATCCACCTGCCT[C/T]GGCCTCCCAAAGGGC | 146845 |
| rs533436803 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9581534 | GAGAGAGAGAGGGGA[A/T]AGAGAGAGAGGAGAG | 146845 |
| rs533530947 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9587455 | ACCACCCTGCTTTCC[A/T]CAATGGTTCAACTAA | 146845 |
| rs533604736 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9592839 | CGTGTACAAGATTTT[G/T]TGTGGACATGTCTTC | 146845 |
| rs533630474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9630849 | AAATTAGCCGGGCGT[A/G]GTGGCGGGAGCCTGT | 146845 |
| rs533663008 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586868 | TTACTTATTTTCTTT[A/T]TTTTTTTTAACTTTT | 146845 |
| rs533665037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9593288 | CCAGAAGAAGGAAGT[A/G]TAACCCTATAGCTGC | 146845 |
| rs533694110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9637061 | AAAAAGCAAACAAAC[A/G]AACAAAAAAGCAAAA | 146845 |
| rs533706165 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9624690 | ATCAGTTGCTTCTGA[C/T]TCTGCCTTTTTTTTG | 146845 |
| rs533745756 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9614587 | GAATTCGTTTATTAT[A/C]AAAATTCATTTGTTT | 146845 |
| rs533751955 | in-del | -/T | 0.00755907 | 0.0610114 | intron-variant | CFAP52 | GRCh38.p7 | 17:9607457 | ATACATTGTCAAGCC[-/T]TTTTTTTCTTTGGAG | 146845 |
| rs533803474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9625920 | TATCTGGCTGATTTC[C/T]ATTTATCCATAATGT | 146845 |
| rs533808971 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9617939 | GGAAGAAACTGCATC[A/C]ACTAATGAGCAAAAT | 146845 |
| rs533868045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9636795 | CTCCCGCCTGTAACC[C/T]CAGCACTTTGGGAGG | 146845 |
| rs533878502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9626510 | ACTGGGATTACAGGC[A/G]TGAGCCACTGCTCCT | 146845 |
| rs533973700 | snp | C/G | 0.000624155 | 0.0176547 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575772 | CCCTCCACGCACCGC[C/G]GCCCTCACCCGGGAC | 146845 |
| rs534018867 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CFAP52 | GRCh38.p7 | 17:9630543 | CACGCCATTCTCCTG[C/T]CTCAGCCTCCCGAGT | 146845 |
| rs534042649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9581178 | AAAAATTAGCCGGGC[A/G]CGGTGGCGGGCACCT | 146845 |
| rs534081177 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9635971 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 146845 |
| rs534129407 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9600165 | AGATGTTGGGCCTGC[A/G]AAGGACAAATTCAGT | 146845 |
| rs534257951 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9606061 | TTTGCTGCAAACCTA[A/C]AACTGCTCTAAAAAA | 146845 |
| rs534323029 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9604599 | ATGGTGAAACCCCGT[C/G]TCTACTAAAAATACA | 146845 |
| rs534324658 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636562 | TTATTTTAGAATCGG[A/G]TGCCATTCCTCCACC | 146845 |
| rs534389264 | snp | C/T | | | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575510 | GGATGGGCGGGAAAT[C/T]CCCGCAACGAGATGC | 146845 |
| rs534413760 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642596 | GCCACTCCACTCCAG[C/T]CTGAGTGACAGACAG | 146845 |
| rs534561803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586208 | CAAACAAAAGTTCCC[A/G]CTTAAAGCTGTTTCC | 146845 |
| rs534572266 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9624149 | GTTTGACTGTGATTT[C/G]TCTTTCTCTTTGTGT | 146845 |
| rs534600177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598011 | AGGTGTGAATCCCTG[C/T]TCTGCTGTGTTCAAG | 146845 |
| rs534747628 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9603840 | TGAAGTATAATTTTT[A/T]AAAAAAGAAAGCACA | 146845 |
| rs534751307 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9595549 | GCCAGGGTTTTATAG[A/G]GTTCTTTCTGCTCCT | 146845 |
| rs534792902 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9591964 | CTATGCAAAAGGATC[A/C]AAAATTCAAAAGCAT | 146845 |
| rs534813417 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9596910 | TTAATAGAGACGGGG[A/T]TTTCACCATGTTGGC | 146845 |
| rs534828452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9589299 | ACAAAGGAAATTTAT[A/G]TTTGTGTATAGTTAT | 146845 |
| rs534837869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9629995 | AGCTCTGGGCTTACC[C/T]TACATCTAGAGCGAA | 146845 |
| rs534896527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9622449 | TAGTCCCAGCTACTC[A/G]GGAGGCTAAGGTGGG | 146845 |
| rs534902812 | in-del | -/TTTG | 0.143491 | 0.226177 | intron-variant | CFAP52 | GRCh38.p7 | 17:9613507 | TTTGGGGGGTTTTTG[-/TTTG]TTTGTTTGTTTGTTT | 146845 |
| rs534912902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9610265 | TAGTAAATTAACCTT[C/T]TAATTTTTTACCCCT | 146845 |
| rs534985512 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9634719 | CAGTGAGCCGAGATC[A/G]CGCCATTGCACTCCA | 146845 |
| rs535015344 | snp | A/G/T | 0.00199529 | 0.0315338 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585532 | AAAAATTAGCCAGGT[A/G/T]TGGTGGCGGGTGCCT | 146845 |
| rs535028367 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CFAP52 | GRCh38.p7 | 17:9621928 | GTTAGTGGGTGCAGC[A/G]CACCAGCATGGCACA | 146845 |
| rs535032091 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9629376 | GCTCAGAAAGTACAC[A/T]TACTGCTTCACATCA | 146845 |
| rs535034738 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CFAP52 | GRCh38.p7 | 17:9634031 | TCAATTATTAAATAC[A/G]CCCAGACGTTTTGAC | 146845 |
| rs535046053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9641389 | TTTCCTCCCTCCAGG[C/T]CTGAAGCTTAGCTGT | 146845 |
| rs535131287 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP52 | GRCh38.p7 | 17:9614778 | TCTACCCATCAGACG[C/T]GAGTAGCAGCTCCTT | 146845 |
| rs535132658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9604763 | TCAAAATAAATAAAT[A/G]AATAAATAAATAAAT | 146845 |
| rs535143904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9592048 | TTTTTTAATTGAAAT[A/G]CATTTCACATATCAT | 146845 |
| rs535181239 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP52 | GRCh38.p7 | 17:9610631 | CCTCCGCCTCCCGGG[C/T]TCAAGAGATTCTCCT | 146845 |
| rs535193471 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9581185 | AGCCGGGCGCGGTGG[C/T]GGGCACCTGTAGTCC | 146845 |
| rs535311443 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9584466 | TGTATCAATTTAAAG[A/T]GTATAACACAATGTG | 146845 |
| rs535348912 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | CFAP52 | GRCh38.p7 | 17:9636249 | AGAAAGAAAGAAAGA[A/G]AGAGAAAGAAAAATA | 146845 |
| rs535405638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9591307 | CCTCCCAAAGTGCTG[A/G]GATTATAGGCTTGAG | 146845 |
| rs535443877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585542 | CAGGTGTGGTGGCGG[A/G]TGCCTGTAATCCCAG | 146845 |
| rs535472390 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9593703 | TCAGGTGATCCACCC[A/G]CCTCGGCCTCCCAAA | 146845 |
| rs535551235 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598609 | TCTACTAAAAATACA[C/G]AAGTAGCCAGGTGTG | 146845 |
| rs535608780 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586470 | CGGGAGGCTGAGACA[A/G]GGAGAAGTGCTTGAA | 146845 |
| rs535646516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9611502 | TGGGACTATAGGTGC[A/G]CACCACCACACCTGG | 146845 |
| rs535727501 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9596954 | AACTCCTGACCTCAG[A/G]TGATCCACCCACCTT | 146845 |
| rs535749124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586250 | GTCATGTTTGTAGAA[C/T]CTGATCCGATTTCTA | 146845 |
| rs535774967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9610998 | TTATTCTGTGGTTGA[A/G]TAAACTGAGGCCAGA | 146845 |
| rs535801662 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9623065 | AGGTCTCAGGCAATG[A/G]ATGTAGAGTTCCACC | 146845 |
| rs535868540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9579797 | GGTCTTGAACTCCTG[A/G]CCTCAGGTGATCCAC | 146845 |
| rs535878214 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9580676 | CCTGGGCAACAGAGT[A/G]AGACCTGGTCTCAAA | 146845 |
| rs535927852 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9592612 | TCATAAGTAGAATCA[C/T]ACAATATGTGGTCTT | 146845 |
| rs535937022 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9640566 | CATGTCCCGGCAAAG[A/G]ACATGATCTTGTTCC | 146845 |
| rs536001016 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9634839 | AAGCATCATATTAAT[G/T]ATTTTAAATTTTGTG | 146845 |
| rs536081262 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9589954 | TCTTCTCCTTCTTGG[C/G]CCGGAGGTGCTCTTC | 146845 |
| rs536108688 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9602829 | AACGTGAGATGGTAT[C/T]GCATTGCAGTTTTGA | 146845 |
| rs536246303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9616531 | CTGCCTCTGTAGGCT[C/T]CACCTCTGGGGGCAG | 146845 |
| rs536285248 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9609504 | GTTCCAGCCCAGCCT[A/G]GGCAACACAGTGAAG | 146845 |
| rs536323952 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9606629 | CAGGCCGACTGGCTG[C/T]AGAACCTGTGCACTT | 146845 |
| rs536360083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9578660 | AAGCTATTCTCCTGC[C/T]TCAGCCTCCAGAGTA | 146845 |
| rs536369160 | in-del | -/CTTATTCAGCAC | 0.0023933 | 0.0345097 | intron-variant | CFAP52 | GRCh38.p7 | 17:9608773 | TGCCATAACAATGTG[-/CTTATTCAGCAC]CTCCTCCAACCAAAC | 146845 |
| rs536369884 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9615018 | AATACTGCAGTAAAT[A/T]TAGGACTTCGCCTTT | 146845 |
| rs536381048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9616007 | GGAGCCAAGATGGCC[A/G]AATAGGAACAGCTCC | 146845 |
| rs536381395 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9601376 | TGTAACAAACCTGCA[C/T]GTTGTGCACATGTAC | 146845 |
| rs536381588 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9608297 | AGCCAGCAACTCGAT[G/T]ATATCGGCAAAGTGA | 146845 |
| rs536423393 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9597078 | CTCCCTACTCTCCCA[A/C]CCCCAGTCTCTGATA | 146845 |
| rs536450751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9627334 | GGCCAACATGGTGAA[A/G]CCCCGTCTCTACTAA | 146845 |
| rs536563136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9603319 | GTTTACGCCATTCTC[C/T]TGACTCAGTCTCCAG | 146845 |
| rs536584900 | snp | C/G | 1.64846e-05 | 0.0028709 | missense | CFAP52 | GRCh38.p7 | 17:9632927 | CCTTCGCCCCAGAGA[C/G]AGGCCGACTGATGTA | 146845 |
| rs536593759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9639145 | TTAAAAATCTACACA[C/T]GGAGCCAAGCGTGGT | 146845 |
| rs536626244 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9619878 | GAGCTATCTATGACA[A/G]ACCCACAGCCAATAT | 146845 |
| rs536632724 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9610715 | AATTTTTTTTTGTAT[C/T]TTTAGTAGAGATGGG | 146845 |
| rs536645670 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CFAP52 | GRCh38.p7 | 17:9594104 | CTGTTGTGTTTTTTT[C/T]TTTCTAGAACCACTA | 146845 |
| rs536648525 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9601902 | TTAGATACTTTTCCA[C/T]ATAGCAGATATTCTC | 146845 |
| rs536687681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642485 | AAAAATTAGCCGGGC[A/G]TGGTGGTGCACGCCT | 146845 |
| rs536782316 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9633317 | TCAAGCGATTCTCCT[A/G]CCTCAGCCTCCTGAG | 146845 |
| rs536826765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9589098 | CAGAGCAAGACTCCA[A/G]CTGAAAATAAATAAA | 146845 |
| rs536859368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633467 | GCCTTGGCCTCCCAA[A/G]GTGCTGGGATTACAG | 146845 |
| rs536866577 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9641131 | CACCCTCCTTTAGGC[A/C]CCTGTCTCTCCATCC | 146845 |
| rs536969230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9588544 | CCTGCCTACAGCCCC[C/T]GAGTGTTCTTTCTGC | 146845 |
| rs537029862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9588610 | TGGACCTGGACCCTG[A/G]GATCTGACAGCATCC | 146845 |
| rs537035068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9603441 | GTCTCGATCTCCTGA[C/T]CCCGTGATCCACCCG | 146845 |
| rs537102478 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9601920 | AGCAGATATTCTCAA[G/T]AAACTTTGAAATACT | 146845 |
| rs537114902 | snp | C/T | 0.275732 | 0.248672 | intron-variant | CFAP52 | GRCh38.p7 | 17:9618990 | GCAGAAGGCAAGAAA[C/T]AACTAAAATCAGAGC | 146845 |
| rs537168116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9595147 | TGTTTGGAGTTTGAA[A/G]GGAAGGTTAAATATG | 146845 |
| rs537201640 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9640643 | CTTAAGTTTATTCTG[G/T]TTTTTTTGGAGACAG | 146845 |
| rs537231276 | snp | A/G | 0 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9590601 | TTAAAAAACACTGAC[A/G]CCTGGGTCCCACCCC | 146845 |
| rs537249920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9616049 | CCCAGCGTGAGCGAC[A/G]CAGAAGACGGGTGAT | 146845 |
| rs537256830 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9635073 | GCAGTGATCAGCAAA[A/T]GTGAATAGACATTAT | 146845 |
| rs537295161 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9597313 | AGGTTATGTACATCA[C/T]GGTGAGTATAGTTCG | 146845 |
| rs537301874 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585596 | GAATCACTTGAACCC[-/A]GGAGGTGAAGGTTGC | 146845 |
| rs537359109 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9597982 | TAGTGTGCACTTCAG[A/T]GTGAGACGGAGCCAG | 146845 |
| rs537386868 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633970 | ACAGGCGTGAGCCAC[C/T]GCGCCTGGCCCATCT | 146845 |
| rs537395333 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638996 | TAGGTACTCAATAGA[-/T]TTGGTTTTTATTATT | 146845 |
| rs537397294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9628285 | CTTCCCTATATTCTT[C/T]TTTTTTTTTTTTGAG | 146845 |
| rs537413920 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9583361 | AATCACATAAAGCAC[C/G]AAAATAAATTCCAGA | 146845 |
| rs537442885 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9626643 | CTCATTCACCAAAGG[C/G]ATTATCTAATATAAA | 146845 |
| rs537491697 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9577314 | TTCTAAATGATGAGG[A/G]TTTCAGACCAGGACA | 146845 |
| rs537494512 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP52 | GRCh38.p7 | 17:9589240 | ATTTAATACTTCAGT[A/G]CACTTCTATGTATAT | 146845 |
| rs537550595 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9582677 | AGTCTCACTCTGTCA[A/C]CCAGGCTGGAGTGCA | 146845 |
| rs537601191 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9578703 | AGCACCCACCACCAC[A/G]CCTGGCTAATTTTTG | 146845 |
| rs537647432 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9640897 | AACGGGCCCAACTCG[A/G]CTTCCCAAAGTGCTG | 146845 |
| rs537714658 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9614664 | ATTGAATTAGGCCAG[C/G]ATTTCTCAACCTCCG | 146845 |
| rs537727485 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9578023 | CTTGAACTTGGGAGG[A/C]AGAGGTTGCAGTGAG | 146845 |
| rs537735055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9578235 | TATTCACCTTGGGAT[A/G]GAGACCTAACATTTA | 146845 |
| rs537736061 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9608418 | TTATGTTGAATCAAA[C/G]CAAAGTAGTCCACTA | 146845 |
| rs537744565 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9588624 | GGGATCTGACAGCAT[C/T]CATATCTTGTTTCAG | 146845 |
| rs537767273 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9598956 | CAGCACATTCCTATG[C/T]CACTGATGCTATTTC | 146845 |
| rs537926886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9637855 | TGCTGGGATTGTAGG[C/T]GTGAGCTGCTGCACT | 146845 |
| rs537978249 | snp | G/T | 0.0097144 | 0.0690133 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632254 | GGCAAGTTTTTTTTT[G/T]TTTTTTTTTTTCATA | 146845 |
| rs538016170 | snp | C/T | 1.65348e-05 | 0.00287526 | synonymous-codon, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643156 | TGTTAGTGTAAGTGC[C/T]GATGGAGCCATTTTG | 146845 |
| rs538089088 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9587487 | CTACTCTCCCACCAA[C/G]AGTACCTAAGCATTC | 146845 |
| rs538122266 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9602273 | TAATGCTATCCCTTT[C/T]CTAGCCCCCACCCCT | 146845 |
| rs538134852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9625293 | TATAATTTAGCTACC[C/T]AGCAGAGACTTGGGC | 146845 |
| rs538166412 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9615084 | AGAAGACTTGAGGCT[G/T]CTGAGTTGTGAATAT | 146845 |
| rs538168762 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600650 | GTTCACAGCAAGCTC[C/T]GCCTCCTGGGTTCAC | 146845 |
| rs538229797 | snp | C/G | | | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9577889 | CTGAGGTCAGGAGTT[C/G]GAGACCATCCTGTCC | 146845 |
| rs538230268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9606088 | AAAAAATAGCCTAGT[A/G]AAAACAAAAATAGTC | 146845 |
| rs538236192 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9613814 | GTGAGCCACTGCACC[C/T]GGCCTCAGACCTCAG | 146845 |
| rs538244156 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9592271 | AGTTCGAGAACAGCC[C/T]GGCCAACATAGTGAA | 146845 |
| rs538266140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9615386 | CTTTTTTCAACTCTT[C/T]ATTTTCAACCTATTA | 146845 |
| rs538267971 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9605664 | TCGCGCCCCTGCACT[G/T]CAGCCTGGCGACAGA | 146845 |
| rs538291858 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9578604 | GCTCTGTTGTGTAAT[A/G]GCACAATCTCGGCTC | 146845 |
| rs538350094 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | CFAP52 | GRCh38.p7 | 17:9580199 | TATTGGAATGTAGCT[-/A]ATGCCCATTTGTTTA | 146845 |
| rs538465375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9637170 | TCATTAAATTTAGCA[C/T]GGTACCTGAGATTCT | 146845 |
| rs538470331 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9593930 | AGATGGCGCCATTGC[A/C]CTCCAGCCTGGGCAA | 146845 |
| rs538483197 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9612289 | GTGAATCTACTTTAC[A/T]TTTGTGCTTCTCCCT | 146845 |
| rs538486368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600201 | GAGTAGAGACCATCG[C/T]CACTGCCCTGCCATT | 146845 |
| rs538578044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9602174 | GATACATGTGCAGAC[C/T]GTGCAGGTTTGTTAC | 146845 |
| rs538649196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9628021 | TTACAGGTGTCAGCC[A/G]CCATATCAGGCCTCA | 146845 |
| rs538712355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632810 | ACCAGGCCTGCCTCT[C/T]CTTAGTGAGGCCAGC | 146845 |
| rs538712809 | in-del | -/TTTG | 0.00743322 | 0.0605091 | intron-variant | CFAP52 | GRCh38.p7 | 17:9613510 | GGGGGTTTTTGTTTG[-/TTTG]TTTGTTTGTTTGTTT | 146845 |
| rs538730404 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9613857 | TGAGCTGTAGTTTCC[A/G]TTCCCTGAATCCCTG | 146845 |
| rs538732918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584237 | AACTCAAGCAAAACA[A/G]TAATTACATTCAAGC | 146845 |
| rs538751897 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9611076 | AACTGAGGTTTAACT[C/T]GTCATCTTCCTTTCG | 146845 |
| rs538792696 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9606796 | TCCTCATAGGCTGAG[C/G]CTTCATCCTGTTGTC | 146845 |
| rs538809756 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CFAP52 | GRCh38.p7 | 17:9637927 | GGCTCTCTTCAGTTG[C/T]GGGAGGCCAGCTCCC | 146845 |
| rs538840534 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9588122 | AGGATAGGCCAAGGT[A/G]GGATGTTTACATCCT | 146845 |
| rs538867143 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9585114 | AGCAGGCTGCTCACA[C/T]TCCATGCATTCGTGC | 146845 |
| rs538909742 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9615988 | ATATAGTTTTTCGGG[A/G]GGAGGAGCCAAGATG | 146845 |
| rs539016338 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642510 | ACGCCTATAATCCCA[C/G]CTACTTGGGAGGCTG | 146845 |
| rs539042987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9592712 | CATTTTTTATCATCA[A/G]ATAGTATTCCATTGT | 146845 |
| rs539162699 | snp | A/T | 0.000131774 | 0.00811601 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9600111 | TGGCACCACGACTGG[A/T]GATATTCTAAAAATG | 146845 |
| rs539167300 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9594082 | TTGTTGTTCGTTTTT[A/G]AGTAACCTGTTGTGT | 146845 |
| rs539198381 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9585540 | GCCAGGTGTGGTGGC[A/G]GGTGCCTGTAATCCC | 146845 |
| rs539202803 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586356 | ATCCCCTGAGGTCAG[A/G]AGTTCGAGACCAGCC | 146845 |
| rs539219250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9594864 | GATTCACTAATTAGA[A/G]CCTTGTTTAAATTAG | 146845 |
| rs539238190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638412 | GGCCAACCGGAGTAC[A/G]CAGAAGTAGAGAGGA | 146845 |
| rs539259232 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9625718 | CTCTTAGAAGAGCAA[A/G]CTCTTCCTGATTTCT | 146845 |
| rs539266285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9588471 | AAGCAGCGGAGGCAG[A/G]GCAGACAGTGTGAGA | 146845 |
| rs539395817 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9625022 | TTTCCAAATATTCTG[A/T]TAACCTCAAGCTCTG | 146845 |
| rs539397527 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9631633 | TAGTTGGGCTAGGGG[C/T]GCAGGGACAGCCAGT | 146845 |
| rs539509968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642025 | GTCACATTTCAATGA[A/G]AGGAAACATTTGCAC | 146845 |
| rs539536442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9592122 | GTGTTCACAAGGTTT[A/G]CAATCATCATCCACA | 146845 |
| rs539601987 | snp | C/T | 0.00109217 | 0.0233429 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575811 | GGTCCGGTGCCATCC[C/T]GCAGACTCCGCCCGC | 146845 |
| rs539719072 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9623794 | CTAAACACCTGGTCT[C/G]AAGTGTTCCTCCTGC | 146845 |
| rs539725507 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9585257 | CTGCATTTTAACAGG[A/G]TCCCTCAGGGATTTT | 146845 |
| rs539728302 | snp | A/C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9574950 | AATATCCAGGATGTG[A/C/G]GCAACTTAAACAATT | 146845 |
| rs539845945 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9612665 | TATATTAGCTTTCCA[A/G]TTCAAATTTGAGTTT | 146845 |
| rs539927074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9629660 | TCAAGCAATTCTCCT[A/G]TCTCAGCCTCCAGAG | 146845 |
| rs539929731 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CFAP52 | GRCh38.p7 | 17:9630714 | GGATTACAGGCGTGA[A/G]CCACTGCGCCCTGCC | 146845 |
| rs539977652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9581321 | GTTAATTTTATGTTA[C/T]GTGAATTTCACTCCA | 146845 |
| rs539980183 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9624363 | TTTTTCTTCAATTTT[A/T]AAAATCTTTTTAAAA | 146845 |
| rs539987493 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9629913 | TCTTTTCTTGGCCCT[A/G]TCTTCTCCTCCTTGT | 146845 |
| rs540077246 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9609275 | CATGGAGCTTACATT[C/T]TAGCAGGAAGGAAAA | 146845 |
| rs540103293 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9613495 | TTGTTTTTTGTTTTT[G/T]GGGGGTTTTTGTTTG | 146845 |
| rs540133583 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585397 | GTGTTGGCCGGGCGC[A/G]GTGGCTCACACCTGT | 146845 |
| rs540134275 | in-del | -/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9640642 | CTTAAGTTTATTCTG[-/T]TTTTTTTTGGAGACA | 146845 |
| rs540161312 | in-del | -/A | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9637072 | AACAAACAAAAAAGC[-/A]AAAAAAAAACCCGAC | 146845 |
| rs540210570 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CFAP52 | GRCh38.p7 | 17:9581806 | TTGGCAGCCAATTGA[A/G]AGATGTAACATAATT | 146845 |
| rs540250393 | snp | A/G | 0.000113837 | 0.00754357 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575825 | CTGCAGACTCCGCCC[A/G]CCGCTCGGACTCTTC | 146845 |
| rs540277541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9604950 | AACAACACCTAATAT[C/T]GACAGAGATGGAGAG | 146845 |
| rs540281525 | in-del | -/GA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9609990 | GGAATCTGATTTCTG[-/GA]GAGAGAGAGAGAGAG | 146845 |
| rs540345170 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9574642 | CGGGTTCAAGCGATT[A/C]TCCTGCCTCAGTCTC | 146845 |
| rs540365164 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9631223 | TTCTGTCCTCCTTTA[C/G]CTTCTTACCTGGAGC | 146845 |
| rs540414055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9606987 | GCAGGATATTTGTTT[C/T]ATCATATTCAAAATT | 146845 |
| rs540425167 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9592163 | GTTTTCAACACCCCA[A/G]AAAGAAACCCCATAC | 146845 |
| rs540490500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9636425 | GCGTATCACACCCCC[A/G]TAGAATGACTAACTT | 146845 |
| rs540543218 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598702 | GGAGGCGGAAGTTGC[A/G]GTGAGCTGGCATCAT | 146845 |
| rs540555328 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9611501 | CTGGGACTATAGGTG[C/T]GCACCACCACACCTG | 146845 |
| rs540645629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9640731 | CTCCTACAACTTTCA[C/T]CTCCTGGGTACAAGT | 146845 |
| rs540711219 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9582155 | AAGGTTATCTCTGGG[A/C]AGGTTGCACACCTAA | 146845 |
| rs540718330 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9628468 | TATTTTTAGTAGAAA[C/T]GGGGTTTCACCATGT | 146845 |
| rs540743640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9603504 | GTGAGCCACCACACC[C/T]GGCCCTAAGTAGATA | 146845 |
| rs540749336 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9604352 | AAGATACAGAGTGAG[A/T]GGAAATATTGGCAAA | 146845 |
| rs540924429 | snp | G/T | 0 | 0 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641613 | AGCCAGTATCATCCC[G/T]TGGTGTATTTTTGCT | 146845 |
| rs540985195 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9627627 | AAATGTTATAGGTGT[C/T]GACTTATCTTCAAAC | 146845 |
| rs541011253 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | CFAP52 | GRCh38.p7 | 17:9629702 | ACAGGCACGCTCCTG[C/T]CTCAGCCTCCCAAGT | 146845 |
| rs541024878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9590085 | TCCGTGAGAATCCAG[C/T]TGTTTTTTGAATACA | 146845 |
| rs541046658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9628382 | CCTTCCAGGTTCAAG[C/T]GATTCTCCTGCCTCA | 146845 |
| rs541091088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638334 | ACTTAAGGGTTCTCA[C/T]TGAGTTTCGTGCTCT | 146845 |
| rs541165594 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9589605 | GGGCATGGTGGCAGG[C/T]GCCTGTAATCCCATC | 146845 |
| rs541216238 | snp | C/T | 3.39997e-05 | 0.00412295 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598372 | GTAACAATTAGCACA[C/T]GTTCCTGTTAGCAGT | 146845 |
| rs541281228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585497 | CATGGTGAAACCCCG[C/T]CTCTACTAAAAATAC | 146845 |
| rs541310723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9616152 | TGCGCGCACCGTGCG[C/T]GAGCCGAAGCAGGTC | 146845 |
| rs541312175 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9629240 | CCATTTAGCATAAAT[G/T]ATAGGCAGCGTGATA | 146845 |
| rs541386196 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9635296 | CAAAGACAGGGAATT[A/C]AAAAAACACAAATCA | 146845 |
| rs541467183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9578815 | CCTCCCAAAGTGCTG[A/G]GATTACAGGCTTGAG | 146845 |
| rs541474310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9588734 | TGTTGAGGTATGCTC[C/T]TTCCATACCCAATAG | 146845 |
| rs541509227 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633077 | ACGCTCTGTTTAGAA[A/C]AACTGCCCTATAGGA | 146845 |
| rs541518294 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9617342 | CTCCAAGAAATATGG[A/G]ACTATGTGAAAAGAC | 146845 |
| rs541537061 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584594 | GATCAACTCTTTTAG[A/C]AGATTAATGCAGTAT | 146845 |
| rs541541744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585476 | GTTCAAGACCAGCCT[A/G]ACCAACATGGTGAAA | 146845 |
| rs541565352 | in-del | -/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9604054 | TACAATGGAAAAAAA[-/G]GATCGTCTTTTTAAT | 146845 |
| rs541601611 | in-del | -/A | 0.0287284 | 0.116357 | intron-variant | CFAP52 | GRCh38.p7 | 17:9634597 | TTGTCTCAAAAAAAG[-/A]AAAAAAAAATACAAA | 146845 |
| rs541731566 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9610137 | TTAAAATAGCAACAA[G/T]CAGGAGAGGAAAGAA | 146845 |
| rs541734167 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9630041 | AAATCTTGGAGTCCT[C/T]ACTGCCTCCCCTTTT | 146845 |
| rs541748556 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9622851 | CACTACCCTCACCCT[C/T]CTACTTACTACCTGA | 146845 |
| rs541755530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9609454 | AATCCCAGCTCTTTG[A/G]GAGGTCGAGGCAAGT | 146845 |
| rs541799339 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9623461 | TATTAAATCTTTATA[A/C]AAACTCCATCAAACT | 146845 |
| rs541820121 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9579364 | GAGAGTGCAGGGCCT[G/T]GTTGCAGAACGGCAA | 146845 |
| rs541822279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9609564 | AGCCAGATGTGGTGG[C/T]ACATACCTGTAGTCC | 146845 |
| rs541822589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9622004 | AAACTTAGAGTATAA[C/T]AAAAAAATAAATAAA | 146845 |
| rs541823114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9629716 | GCCTCAGCCTCCCAA[A/G]TATCTGGGACTACAG | 146845 |
| rs541890238 | in-del | -/T | 0.350546 | 0.22889 | intron-variant | CFAP52 | GRCh38.p7 | 17:9640225 | CCTGGTCAAGCACTC[-/T]TTTTTTTTTTTTTTT | 146845 |
| rs541957582 | snp | A/C/G | 0.0460142 | 0.144533 | intron-variant | CFAP52 | GRCh38.p7 | 17:9616218 | GGGAGTTCCCTTTCC[A/C/G]AGTCAAAGAAAGGGG | 146845 |
| rs541972485 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9614503 | TTAGTCTGATATTAA[C/G]ATTACCACATCTTCA | 146845 |
| rs542012413 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9604005 | AAACATGAATTCACA[C/T]AGTCAACTGATCATT | 146845 |
| rs542046369 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9611888 | TAGGTTGTTTCCAAC[A/C]TTTTACTCTTTCAGA | 146845 |
| rs542046458 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9589232 | TGTGTGGGATTTAAT[A/T]CTTCAGTACACTTCT | 146845 |
| rs542055331 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | CFAP52 | GRCh38.p7 | 17:9640389 | TCCTGATGCTCTTCC[C/T]CCCCCCACCCACCAC | 146845 |
| rs542082666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9622840 | CCCCTTCCAATCACT[A/G]CCCTCACCCTCCTAC | 146845 |
| rs542086100 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9610404 | AATTAAATCAGATGC[A/G]GTGGTTTCCACCTGC | 146845 |
| rs542144873 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9594682 | GATTGGGGTCTCATG[A/C]TCTGATAGTTTGCAA | 146845 |
| rs542146496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9580778 | AAAAAGGGTAATATA[A/G]TAAGGTGAGAATAAG | 146845 |
| rs542285947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9628440 | ATGCACCACCATACC[C/T]GGCTAATTTTTGTAT | 146845 |
| rs542333105 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9578854 | CCCAGCCACAGGGTG[A/G]AGGGGTGCATGGCCT | 146845 |
| rs542398247 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP52 | GRCh38.p7 | 17:9597587 | AAGCGGATGGATCAC[A/G]AGGTCAAGAGATGGA | 146845 |
| rs542422739 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9626784 | CTCTTTCTAACTAAG[C/T]AGTCCATCATTATAA | 146845 |
| rs542535256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9603515 | CACCCGGCCCTAAGT[A/G]GATATTTCATGTTCA | 146845 |
| rs542597023 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP52 | GRCh38.p7 | 17:9602234 | TGCACCCATTAACCC[A/G]TCGTCTACATTAAGT | 146845 |
| rs542633582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9637993 | CTTGGGAGGGACTTC[C/T]TACCATATGCAGACA | 146845 |
| rs542661160 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9581748 | CTGGTTCTATTGCTT[C/T]AGTGAGAGCCTAAAA | 146845 |
| rs542712515 | snp | A/G | 0.000115644 | 0.0076032 | missense | CFAP52 | GRCh38.p7 | 17:9608150 | GGTGCCTGAAGATGG[A/G]GGGTTTGTTGGTGGG | 146845 |
| rs542804656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9639526 | AATGTTCACCCTTGG[A/G]GCAAGCAAGGGGTCC | 146845 |
| rs542822077 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633725 | TCTGTCACCCAGGCT[A/G]GACTGCAGTGGCACA | 146845 |
| rs542860579 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9595284 | CTTGGAAAGGTACAC[A/G]TGGTTGGTTACTTTT | 146845 |
| rs542901507 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9579107 | GGGGCAGCGTGGGGA[C/T]TGGGGAGCTTATGAT | 146845 |
| rs542941463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638788 | TGGTGGAGGGTGCGG[A/G]CTCTGGAGTCAAACC | 146845 |
| rs543094765 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9601276 | GTGGGGTGGGGGGAG[C/G]GGGGAGGGATAGCAT | 146845 |
| rs543096704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9593036 | ACTTCCTACCTCCCT[A/G]TTCCTGGTGATCTTG | 146845 |
| rs543157320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9593558 | CCTCCCGGATTCAAG[C/T]GATTCTCCTGCCTCA | 146845 |
| rs543181533 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9627335 | GCCAACATGGTGAAA[A/C]CCCGTCTCTACTAAA | 146845 |
| rs543186363 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9595363 | GTCCCCGCTTTATGA[C/T]ATGCAACTTACATTT | 146845 |
| rs543193405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585494 | CAACATGGTGAAACC[C/T]CGTCTCTACTAAAAA | 146845 |
| rs543207710 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9578950 | AACATTAATGCTGAT[C/G]AGTTGTGTCTAAACC | 146845 |
| rs543249020 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9614754 | GGATGTTTGGCAGCA[A/T]TCCTGGGCTCTACCC | 146845 |
| rs543327939 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9593890 | GAATCGCTTGAATCC[A/G]GGAGGCGGAGGTTGC | 146845 |
| rs543330425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9583758 | TCAAAAAAATTCTGA[C/T]CATAGGTGAGCAATA | 146845 |
| rs543331775 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585393 | TAAAGTGTTGGCCGG[A/G]CGCGGTGGCTCACAC | 146845 |
| rs543346966 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9626827 | GCCCCAAGCATTAAA[C/T]GTGTGGAAGGGATCC | 146845 |
| rs543370295 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9590023 | CCTGAGCCTGTTCAG[C/T]TGGGAGCTTTTCACA | 146845 |
| rs543372974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632517 | AGCTGTTATCACAAT[C/T]CAGGAGAAAGATGGT | 146845 |
| rs543410473 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9593412 | AACTGCGGTGCTGTG[A/G]CCTAGCAGTCTCTGT | 146845 |
| rs543433077 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9639669 | GATGAGATGGTGAAA[C/G]GACTGAGAAAGGAGA | 146845 |
| rs543595021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9634348 | GACAGATCCTTTGTC[C/T]ATTAAAGGAATACTG | 146845 |
| rs543603225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9628529 | GTGATCCACCCCCCT[A/G]GCCTCCCAAAGTGCT | 146845 |
| rs543738556 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633825 | GGGACTACAGGTGCC[C/T]GCCACCACGCCCAGC | 146845 |
| rs543744116 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9614881 | GCTGAGAATCACTGG[G/T]GTTAGGCCAGACCTC | 146845 |
| rs543746221 | in-del | -/T | 0.29278 | 0.246313 | intron-variant | CFAP52 | GRCh38.p7 | 17:9627112 | TATTTAGAGGTTGCC[-/T]TTTTTTTTTTTTTTT | 146845 |
| rs543818378 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9637417 | CAGATACCACGTTTG[A/G]AAACTTCCATAATGA | 146845 |
| rs543830976 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9630583 | TACAGGCGCCCGCTA[C/T]CACGCCCGGCTAATT | 146845 |
| rs543877873 | snp | A/C/G | 0.000115587 | 0.00760132 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584398 | GAACTGAAACCGAAA[A/C/G]TTAAAAAAATTATTT | 146845 |
| rs543913232 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9588210 | TTGCCATAGCATGGG[A/G]AAGGCCATCACTTGG | 146845 |
| rs543928042 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9601491 | CTTTGTGATTTTAAA[C/T]TGCGTTGGTTCCAGC | 146845 |
| rs543931169 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9612040 | GGAATATTCCCTCTA[C/T]CCAAATCCTGCCTGC | 146845 |
| rs543994855 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9601445 | AAAGTACCACATTTA[G/T]GTTCACCTCTTCAAA | 146845 |
| rs543996792 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575842 | CGCTCGGACTCTTCC[C/T]GCTCTTAGCAGCTGA | 146845 |
| rs544040172 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9608725 | TTTCTTGGCTCATTT[A/G]ATTAAAATAAAATGA | 146845 |
| rs544065782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9607135 | AGGATCACTTCAGGT[A/G]AGGAGTTCGAGACCA | 146845 |
| rs544097440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585439 | TTTGGGAGGCTAAGG[C/T]GGACGGATCACGAGG | 146845 |
| rs544129500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600961 | ATTTCCAGTTCTGTG[A/G]AGAAAGTCATTGGCG | 146845 |
| rs544149483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9578420 | AAATTGTTCTTATGG[C/T]GGGTTGAACAGGGCT | 146845 |
| rs544149688 | in-del | -/T | 0.00557542 | 0.0525036 | intron-variant | CFAP52 | GRCh38.p7 | 17:9590664 | CCCAATCCCACCCCC[-/T]GTCAAAGAGACTAGG | 146845 |
| rs544154897 | snp | C/T | 1.6654e-05 | 0.00288561 | missense, upstream-variant-2KB, utr-variant-5-prime | CFAP52, STX8 | GRCh38.p7 | 17:9576709 | GGATGGATAACAAAA[C/T]TTCGCCGGAGGCCCA | 146845 |
| rs544197702 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9614045 | TTGGCCCTGGTGCTT[G/T]TTTTAAGGGTAGATT | 146845 |
| rs544273377 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CFAP52 | GRCh38.p7 | 17:9599747 | AGTTTTCTTCTTCTT[C/T]TTTTTTTTCCTGAGA | 146845 |
| rs544376943 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586963 | GTACAGATTATTTCA[A/T]CAACCAGGTGCTCAG | 146845 |
| rs544440355 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9614481 | TTTCTCTTGCCATCA[A/G]TTTTACTTAGTCTGA | 146845 |
| rs544443053 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP52 | GRCh38.p7 | 17:9581929 | GGTCTTTAGTTCGTG[C/T]CACTTGGTCTCGCCT | 146845 |
| rs544527773 | snp | A/G/T | 0.00398763 | 0.0445073 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586132 | TCATTCCGTCAGACC[A/G/T]GGAGTGAAGGACTCT | 146845 |
| rs544533550 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9592325 | AAAAAAATTAGCTGG[C/G]CGTGGTGGTGGTGGG | 146845 |
| rs544534881 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9623726 | GGTTTCACTCTGTTG[C/T]CCAGGATGGAGTCAA | 146845 |
| rs544569912 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9591185 | TGGGATTACAGGCAT[A/G]CACCACCATGCCTGG | 146845 |
| rs544679690 | snp | A/G | 1.66032e-05 | 0.0028812 | intron-variant | CFAP52 | GRCh38.p7 | 17:9612503 | AAGAGAAAAACAAGA[A/G]TGTGGAGATTTGATG | 146845 |
| rs544681483 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9605024 | ACGGCCACTTTGGAA[G/T]ATAGTTTGGTGGTTT | 146845 |
| rs544722035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9599011 | CCATGAAATCCATTG[C/T]TGAAATGCAATCTCT | 146845 |
| rs544759661 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9614216 | GCTGGAGTGCAGTGG[C/T]ACGATCTTGGCTCAC | 146845 |
| rs544778705 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9636871 | CCAACATGGTGAAAG[A/C]CCGTCTCTACTAAAA | 146845 |
| rs544798497 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9595182 | TTAGAAATCCTTTTT[A/T]AATGTTATATACCAG | 146845 |
| rs544832337 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9631333 | TTGCTCTGACTCTTA[C/G/T]GTCTGCCTGAAATAT | 146845 |
| rs544873828 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9588272 | ATTGCCCTGTGGACA[A/C]TGTGCAGGTGCCCTG | 146845 |
| rs544947012 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9639319 | GCCTGTAATCTCAGC[C/T]ACTCAAGAGGCTGAG | 146845 |
| rs544995890 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP52 | GRCh38.p7 | 17:9607944 | CACTGGCATGACTTT[A/G]GCCATCTTTAATTCA | 146845 |
| rs545082677 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9599987 | CTCAGGTGATCCACC[C/T]GCCTCGGCCTCCCAA | 146845 |
| rs545122464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9640154 | AACACAGCACGTTTC[C/T]GACATGAAACAATGA | 146845 |
| rs545133684 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9614721 | CTTGATATTGTGGAT[A/G]CTATTCTGTGCATTA | 146845 |
| rs545189253 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575940 | AAGTGAGTAGCTAGG[A/G]CCTCAGAACTATAAT | 146845 |
| rs545226350 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576823 | GGAGGACGTGTAGTG[C/G]AAACAGGAATAGTGA | 146845 |
| rs545248121 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9604474 | CTCCCCTAAAGAAGA[C/T]ATACAGATGGCAGCC | 146845 |
| rs545336032 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9587014 | TTTTCTGATCCTCTC[C/T]CTCTCCCACCCTCCA | 146845 |
| rs545397978 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CFAP52 | GRCh38.p7 | 17:9582126 | ATCTGAAGAAATACA[C/T]ACCTGCATGTTACAA | 146845 |
| rs545414660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9593004 | GTGGAAAAGGGAGAA[C/T]TTATGGCTATTATAT | 146845 |
| rs545432437 | in-del | -/T | 0.00953873 | 0.0683987 | intron-variant | CFAP52 | GRCh38.p7 | 17:9595660 | ATATTAAAAAAAAAG[-/T]TTTTTTTAGGACAAT | 146845 |
| rs545459070 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9606243 | TTAAAAATTAGCCGG[C/T]GTGGTGGCATGCATC | 146845 |
| rs545477861 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9581551 | GAGAGAGAGGAGAGG[A/G]AGGGAGGGACAGAGG | 146845 |
| rs545489258 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642315 | TGCCAAGCTCTTTGA[A/T]TCATCAGGATATTAA | 146845 |
| rs545516132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9592430 | GCCAAGATTGCCCCA[C/T]TGCACTCCAGCCTAG | 146845 |
| rs545538924 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9591325 | TTATAGGCTTGAGTC[A/G]CCGCTCCCGGCCTGC | 146845 |
| rs545552036 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600282 | AGTCTTGTTCTGTCA[C/G]TCAACCTGGAGTACA | 146845 |
| rs545574845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9625275 | GTATTCCCCCCATAC[A/G]TATATAATTTAGCTA | 146845 |
| rs545576719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632015 | TGTCCTCAAGTGATC[C/T]GCCTGCCTTGGCCTC | 146845 |
| rs545600319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586123 | AACCCATTTTCATTC[C/T]GTCAGACCGGGAGTG | 146845 |
| rs545675340 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9637276 | CCTTCCTCCTGGGAA[A/C]ATATAGAACTAGAAG | 146845 |
| rs545692087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9605653 | TTGAGCCGAGATCGC[A/G]CCCCTGCACTTCAGC | 146845 |
| rs545703911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9587595 | TTATCTCATTGTGGT[C/T]TTACTTTGCATTTCT | 146845 |
| rs545797466 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9580862 | CAGTTTTATAGTATC[A/T]ATTACAATTCTTAAT | 146845 |
| rs545800983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9603558 | CTCAGTATTGTCACG[A/G]TATGAGTTCTTCTTA | 146845 |
| rs545806261 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9623162 | TTATATCTTTTTGCT[A/G]TATTGACATTTTTAT | 146845 |
| rs545888322 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9611091 | TGTCATCTTCCTTTC[A/G]TCATTAACTGTTCTG | 146845 |
| rs545920758 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9589554 | CCTAGCCAACATGGC[A/G]AGACCCCATCTCTAC | 146845 |
| rs546061622 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9604207 | CTCCTGAAAGATAAA[A/T]TCCAGAAGACCTAAG | 146845 |
| rs546109847 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641508 | TTATCAGCACATCAA[C/G]ATGTCTTTAAATAGA | 146845 |
| rs546121129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598109 | ATAAAAGATCTTTCA[C/T]AGTGCACTAGGCCAT | 146845 |
| rs546139135 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575521 | AAATCCCCGCAACGA[C/G]ATGCAGCCCAGAAAA | 146845 |
| rs546215531 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9601218 | ATTGAACAATGAGAA[C/T]ACATGGACCCGGGAA | 146845 |
| rs546326606 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CFAP52 | GRCh38.p7 | 17:9610486 | GGAAAGGGAAGATGT[A/G]TGATCAAAATGGACA | 146845 |
| rs546332928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9612078 | AACCCATGTCAAAAC[A/G]TTATCTCACTGAAGA | 146845 |
| rs546361768 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642445 | CCTGGCCAACATGGT[A/G]AAACCCTGTGTCTAC | 146845 |
| rs546426291 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9605309 | GACTTTATAGGAAAA[A/G]AAGGAAACTGAGATG | 146845 |
| rs546483589 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9581773 | CTAAAAGAGGCACAT[A/G]TTTTCTCTCCTAATT | 146845 |
| rs546542443 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9599261 | CTCAACAATTTCCGA[C/T]TTTGGAGCATTTCAG | 146845 |
| rs546637037 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9607674 | GTGGCAGCTGAGAGA[C/T]TAGCATTGCTGAGGT | 146845 |
| rs546719804 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9574788 | ATCTGCCTGCCTCGG[C/G]CTCCCAAAGTACTGG | 146845 |
| rs546746635 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | CFAP52 | GRCh38.p7 | 17:9636183 | CTGTCTCAAAAAAAA[A/G]AAAGAAAGAAAGAAA | 146845 |
| rs546807255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586236 | TCCATTGTGTTGCTG[C/T]CATGTTTGTAGAACC | 146845 |
| rs546807331 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9592504 | AAGAAACCCCGTACC[A/C]ATTAGCAATCACTCT | 146845 |
| rs546861310 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9610802 | CCTTGGCCTCCCAAA[C/G]TGCTAGGATTACAGG | 146845 |
| rs546863786 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9591113 | CATGATCTCAGCTCA[C/T]CACAACCTCTGCCTC | 146845 |
| rs546868184 | in-del | -/TTTG | 0.0815733 | 0.18475 | intron-variant | CFAP52 | GRCh38.p7 | 17:9623674 | GCTTAGCTTTTTTTG[-/TTTG]TTTGTTTGTTTGTTT | 146845 |
| rs546877900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9580440 | CACCTGTAATCCCAG[C/T]ACTTTGGGAGGTTGA | 146845 |
| rs546882401 | in-del | -/TT | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9588775 | GCCACAGAAAAGAAT[-/TT]TTTTTTTTTTTTTTG | 146845 |
| rs546899887 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600000 | CCCGCCTCGGCCTCC[C/G]AAAGTGCTGATATTA | 146845 |
| rs546975663 | snp | C/T | 1.64741e-05 | 0.00286998 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9635434 | GATAGGCTGTCAGAC[C/T]CAGAAGCTGGAGGAG | 146845 |
| rs547105592 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9583969 | AGACAATAAACTAGC[A/G]TTCAAAGACCACCTC | 146845 |
| rs547181226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9615027 | GTAAATATAGGACTT[C/T]GCCTTTTAATAAGTA | 146845 |
| rs547278556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9610595 | GCTGGAGTGCAATGA[C/T]GCCATCTTGGCTCAC | 146845 |
| rs547284044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9579770 | ACGGTGTTTCGCCAC[A/G]TTGGCCAGGCTGGTC | 146845 |
| rs547314501 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9609256 | AAAAAAAAATCCCTG[A/T]CCTCATGGAGCTTAC | 146845 |
| rs547338768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9579010 | TCTGACCTCCCATTC[C/T]GTCAAGGCTGGGAAC | 146845 |
| rs547346116 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9614965 | AATAAACTATTAGCA[C/T]AGTTAGAAAGAGTTT | 146845 |
| rs547505788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584813 | TTTTTAGTAGAGACC[A/G]GGTTTCACCATGTTG | 146845 |
| rs547675219 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9599304 | TAGATTTTTGGATTA[C/T]ACTCAACCTGTATAA | 146845 |
| rs547684733 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9588473 | GCAGCGGAGGCAGGG[A/C]AGACAGTGTGAGAAA | 146845 |
| rs547693264 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9616409 | AACTGCAAGGCGGCA[A/G]CGAGGCTGGGGGAGG | 146845 |
| rs547745571 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9635827 | AGTGAAGCATGGTTT[A/T]ACTTACACGAATTCA | 146845 |
| rs547762556 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9596956 | CTCCTGACCTCAGGT[C/G]ATCCACCCACCTTTG | 146845 |
| rs547823166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9602370 | ATGAATGAGAACATG[C/T]GGTGTTTGGTTTTCT | 146845 |
| rs547825266 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CFAP52 | GRCh38.p7 | 17:9629310 | TTTTCCTTTAAAACA[A/G]TAATTTCTCAGTATT | 146845 |
| rs547908008 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9638110 | CTGTGTACAAATGTG[C/T]ACATGACATCTTGCT | 146845 |
| rs547980437 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CFAP52 | GRCh38.p7 | 17:9613665 | TAGGATTACAGGCAT[A/G]CACCACCACGCCCGG | 146845 |
| rs548020282 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9595468 | ACCAAGCAACCTAAA[A/G]CAACTGACCACGGGC | 146845 |
| rs548041082 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9636645 | TATATCACTGCATAC[A/G]AGAGACGAGGATAAG | 146845 |
| rs548072008 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9579385 | AGAACGGCAAATAGC[G/T]TGGGGTGGCTTCAGT | 146845 |
| rs548129650 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | CFAP52 | GRCh38.p7 | 17:9618144 | GGCTCAAAATAAAAG[A/G]ATGGAGGAAGATCTA | 146845 |
| rs548217420 | in-del | -/AAAAAAA/AAAAAAAA/AAAAAAAAA | 0.466515 | 0.124985 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598760 | GTGACACTCTGTTTC[-/AAAAAAA/AAAAAAAA/AAAAAAAAA]AAAAAAAAAAGAAGA | 146845 |
| rs548229231 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9624902 | TTTTAGCCTGGCCTT[C/G]GGTTCTTCTGTGTGC | 146845 |
| rs548253635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9608330 | TTTGGTTAAAAAATT[C/T]CATCTTGCTGTTAGA | 146845 |
| rs548276682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9579100 | CTGGGGTGGGGCAGC[A/G]TGGGGATTGGGGAGC | 146845 |
| rs548312169 | snp | G/T | 4.9445e-05 | 0.00497193 | missense | CFAP52 | GRCh38.p7 | 17:9594296 | TTCTCCAGGTGCCGG[G/T]ATGAGATGTTTATGA | 146845 |
| rs548320520 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585510 | CGTCTCTACTAAAAA[C/T]ACAAAAAAAAATTAG | 146845 |
| rs548323340 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9615855 | ATGTTGCCCAAGCTG[C/G]TTTTCAACTGCCATC | 146845 |
| rs548405890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9604489 | TATACAGATGGCAGC[C/T]GGGCGCAGTGGCTTG | 146845 |
| rs548411312 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633956 | AAAGTGCTGGGATTA[C/T]AGGCGTGAGCCACCG | 146845 |
| rs548474175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9639152 | TCTACACACGGAGCC[A/G]AGCGTGGTGGCTGAT | 146845 |
| rs548544449 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9611239 | AGGGCCTCATTCATG[C/T]ATATACTTTTTTTTT | 146845 |
| rs548569133 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9603229 | GTTATTATTTTTTGA[A/T]ACAGAGTCTCGCTCT | 146845 |
| rs548618431 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9602772 | CCACATCCTCCCCAG[C/G]ATCTGTTGTTTCCTG | 146845 |
| rs548708386 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636305 | ATTCCAGTTAGTCAG[C/G]TGAAGCCCAGAATGA | 146845 |
| rs548817210 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9588365 | GGACACAGCTCAGCC[A/C/T]GCTCGTGCCCAGAGA | 146845 |
| rs548832293 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CFAP52 | GRCh38.p7 | 17:9595490 | ACCACGGGCTGTGGC[A/G]ACACTCTTCAACTTT | 146845 |
| rs548880193 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584089 | TCAATATGTTGGGGC[C/G]TTCTGCAGATGCCAT | 146845 |
| rs548974371 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9637651 | ATGATCTTGGCTCAC[A/T]GCAGCCTCTGCCTCC | 146845 |
| rs549026296 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9601080 | TGGAATACTATGCAG[C/G]CATAAAAAAGGATGA | 146845 |
| rs549062848 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9636932 | TGCCTGTTATCCCAG[A/C]TACTCAGGAGGCTGA | 146845 |
| rs549088236 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9593896 | CTTGAATCCAGGAGG[C/G/T]GGAGGTTGCAATGAG | 146845 |
| rs549129536 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9605076 | TTACCATGTAATGCA[G/T]CAGTTGCACTCCTTG | 146845 |
| rs549166419 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9602223 | TGGTGGTTTGCTGCA[C/T]CCATTAACCCGTCGT | 146845 |
| rs549222881 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9581668 | ATTGTAGTGGACATG[C/T]GTAGTTTTGGTTACT | 146845 |
| rs549247981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632723 | GGTGGTGGCAACCTG[C/T]AGAAGGGAAAGGGGC | 146845 |
| rs549293820 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9593315 | CTGCAATTCTCACAA[C/T]GTGGTTCCCAGACCA | 146845 |
| rs549311286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9631539 | AGAGGGAATAGCAAG[C/T]GCAAAGGCCCTCAGG | 146845 |
| rs549335472 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9582172 | GGTTGCACACCTAAG[A/G]ATAGAGTAGCTGGGT | 146845 |
| rs549372635 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9625427 | CTAGCATTGTTAGCT[A/G]GGGATACATGTATAA | 146845 |
| rs549394423 | in-del | -/TTTGTTTG | 0.0290784 | 0.11702 | intron-variant | CFAP52 | GRCh38.p7 | 17:9613503 | TGTTTTTGGGGGGTT[-/TTTGTTTG]TTTGTTTGTTTGTTT | 146845 |
| rs549449085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9606611 | AGAGCTGAGATTTCA[A/G]CCCAGGCCGACTGGC | 146845 |
| rs549588867 | in-del | -/GTTCATTTAACATCTT | 0.00279162 | 0.0372561 | intron-variant | CFAP52 | GRCh38.p7 | 17:9623858 | ATGCCATTTTGCCTG[-/GTTCATTTAACATCTT]TTTAAAAGTATAAGC | 146845 |
| rs549604836 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9607266 | CACAAGAATCGCTTG[A/C]ACTTGGGAGGCAGAG | 146845 |
| rs549632689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9578290 | TGTCAAAAGGCCTTT[C/T]CAGGACATGACGGCA | 146845 |
| rs549674604 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CFAP52 | GRCh38.p7 | 17:9613799 | GTTGGGATTACAGGC[A/G]TGAGCCACTGCACCC | 146845 |
| rs549733797 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9616334 | TATATCCCACACCTG[A/G]CTCAGAGGGTCCTAC | 146845 |
| rs549852776 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638365 | GTCTTTAGGAAAGGG[A/C]CCTTCCCATTGTCCT | 146845 |
| rs549861851 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632103 | CTTTTTTTGAGACAG[G/T]GTCTTGCTCTGTTGC | 146845 |
| rs549879460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9588436 | CTGGCTGCGCAGCTG[C/T]ATGTGGGAGATGCCA | 146845 |
| rs550055108 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9628210 | TTAAATACCGTTTAC[A/C]CAAGATGTTTCAAAT | 146845 |
| rs550085289 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB, intron-variant | CFAP52, USP43 | GRCh38.p7 | 17:9643846 | GAAATTACAGAGATG[C/T]TTTATTGGAGTTGGC | 146845 |
| rs550109203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9626374 | AGCTGGGACTACAGG[C/T]GCACACCACCACACC | 146845 |
| rs550116476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9593982 | AAAAGAAACAATAAC[A/G]ACAACAACAAAAAAC | 146845 |
| rs550138562 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9625371 | ACTAGGATATTCCCC[C/G]TTTAAATTCCAGCTG | 146845 |
| rs550247570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9605221 | TAAGTAAAGGGATAC[A/G]TAAACTGTGATACAT | 146845 |
| rs550263060 | in-del | -/T | 0.00770623 | 0.0615933 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632255 | CAAGTTTTTTTTTGT[-/T]TTTTTTTTTTCATAT | 146845 |
| rs550314385 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600011 | CTCCCAAAGTGCTGA[G/T]ATTACAGGCGTGAGC | 146845 |
| rs550327307 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9636999 | GCAGTGAGCTGAGAT[A/C]GCACCACTGCACTCC | 146845 |
| rs550346897 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642495 | CGGGCGTGGTGGTGC[A/T]CGCCTATAATCCCAG | 146845 |
| rs550425884 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600429 | GTATTTTTTAGTACA[C/G]ACAGGGTTTCATCAT | 146845 |
| rs550443039 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | CFAP52 | GRCh38.p7 | 17:9597382 | AGTATTCTCACCGCC[-/A]AAAAAAATGGTAAGT | 146845 |
| rs550464162 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9581850 | AGACATTCCCACTCC[A/G]CAGTTCCACTCTTAT | 146845 |
| rs550464961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9636746 | ATGTGTACTTAATAC[A/G]TTAAAAAACACAAAG | 146845 |
| rs550482311 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9607325 | CACTCCAGTCTGAGT[G/T]ACAGAGAGAGACTCT | 146845 |
| rs550525198 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CFAP52 | GRCh38.p7 | 17:9605484 | TGTGGGGAGCTGAGA[C/T]GAGCAGATCATGAGG | 146845 |
| rs550539742 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9601194 | ACATTTTCTTACTCA[C/T]AGGTGGGAATTGAAC | 146845 |
| rs550571852 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9592618 | GTAGAATCATACAAT[A/G]TGTGGTCTTTTGTGA | 146845 |
| rs550616327 | in-del | -/TTTT | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9613501 | TTTGTTTTTGGGGGG[-/TTTT]TGTTTGTTTGTTTGT | 146845 |
| rs550783992 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP52 | GRCh38.p7 | 17:9612214 | GGCGTGTCTGAAATT[A/G]TATGCCTGATTTGTA | 146845 |
| rs550787115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9587226 | ATGGCTGCGTAGTAG[C/T]CCATGATGTATATGT | 146845 |
| rs550816326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586158 | ACTCTGATGATTTTA[C/T]ACCCGAGGTTGCAGC | 146845 |
| rs550816637 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9580569 | CGATGCATGCCTGTA[G/T]TCCCAGCTATTCGAG | 146845 |
| rs550824222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9591178 | AAACAGCTGGGATTA[C/T]AGGCATGCACCACCA | 146845 |
| rs550856993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9623747 | ATGGAGTCAAGTGTC[C/T]ATTCACCCGCATGAT | 146845 |
| rs550879785 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP52 | GRCh38.p7 | 17:9581032 | AGTTTTAAAAAACTA[C/T]GTGGCCAGGCGTGGT | 146845 |
| rs550880949 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9593119 | TTGGGAAATATAGTT[A/T]GGTATGTTTTTACAT | 146845 |
| rs550925658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586499 | AACCCAGGAGGTGGA[C/T]GTTGCAGTGAGCAGA | 146845 |
| rs550957969 | snp | A/G | 1.64898e-05 | 0.00287135 | missense, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641745 | TACTGGGAAGTATTT[A/G]ATGGGACAGTAATCA | 146845 |
| rs550989931 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9630350 | TTGGAGGCCGAGGCG[G/T]GAGCCACCGCACCTG | 146845 |
| rs551047571 | snp | A/G | 1.64727e-05 | 0.00286986 | missense | CFAP52 | GRCh38.p7 | 17:9600136 | AAAATGAACCCCAGG[A/G]CTAAACTGCTGACAG | 146845 |
| rs551110715 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600481 | CTCCTGACCTCAAGT[C/G]ATCTGCCCACCTTGG | 146845 |
| rs551254514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9631671 | GTTAAAAGAGATGGC[A/G]GGGGTTGGGGGTCGG | 146845 |
| rs551357433 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9604394 | AATAAGGACTGTTAC[C/T]CAAAATATACAGAGA | 146845 |
| rs551358677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9581174 | ACCAAAAAATTAGCC[A/G]GGCGCGGTGGCGGGC | 146845 |
| rs551359555 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9587310 | GTCTTTGCTATTGTG[A/G]ATAGTGCTGTGATGC | 146845 |
| rs551428562 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB, intron-variant | CFAP52, USP43 | GRCh38.p7 | 17:9643713 | GTTATTGTGAGAATT[A/C]AGTGACTAATGTACT | 146845 |
| rs551439945 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9606507 | GATCTTCATAAACGC[C/T]TAATGAGATAGGTAC | 146845 |
| rs551550510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9583123 | AATTATGAATCTAAG[C/T]TTAATTTTTCCATAT | 146845 |
| rs551555306 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9591859 | CTCCAGCTGGGGCAA[C/G]AGAGAGAGACCTTGT | 146845 |
| rs551589859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9636088 | CTGAGGCAGGAGAGT[C/T]GCTTGAACCCAGGAT | 146845 |
| rs551616881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9581572 | GGGACAGAGGGAGAC[A/G]GAGAGGGAGGGAAAG | 146845 |
| rs551617106 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586181 | GTTGCAGCTTGTGAC[C/T]GATAATGCTCACAAA | 146845 |
| rs551624820 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9574991 | TTAGAAATAACAACA[C/T]AAGACACATATTCCA | 146845 |
| rs551641880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9612811 | TATGATTTTTTTTAT[C/T]TTATGATGGTGTAAA | 146845 |
| rs551646669 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9637584 | ATGCACATAAAAATC[A/C]ACTGAAATGCTGGTT | 146845 |
| rs551719735 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | CFAP52 | GRCh38.p7 | 17:9636606 | ACCTATCACCCCTCT[A/C]CCCCTCCTACGAGGC | 146845 |
| rs551769503 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | CFAP52 | GRCh38.p7 | 17:9630460 | TAAGAGACGGAGTCT[C/T]TTTCTGTCTCCCAGG | 146845 |
| rs551772760 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576594 | AGGCTGGGTTTCTGC[A/G]CGGGCGTGGAGCTGG | 146845 |
| rs551802500 | in-del | -/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9640224 | TCCTGGTCAAGCACT[-/C]TTTTTTTTTTTTTTT | 146845 |
| rs551830944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9630918 | TTGAACCCGGGAGGT[A/G]GAGGTTGCAGTGAGC | 146845 |
| rs551832787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9623819 | TCCTGCCTCAGCCTC[C/T]TGAGTAGCTGGGACT | 146845 |
| rs551905345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9611332 | AACTCCTTAAGGTTC[C/T]GGCAAAGACAACCCC | 146845 |
| rs551912189 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9592792 | GTCATTTCCACTTCT[A/T]AATTATTATTAATAA | 146845 |
| rs552097211 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9624704 | ACTCTGCCTTTTTTT[G/T]GAGTCATATTTTCCT | 146845 |
| rs552108708 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9610775 | AACTCCTGACCTCAG[A/G]TGATCCACCCACCTT | 146845 |
| rs552119987 | snp | A/G/T | 8.23885e-05 | 0.00641781 | missense, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641773 | TCAGAGAATTGGAAG[A/G/T]TTCCCTGTCTGGGTC | 146845 |
| rs552245995 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CFAP52 | GRCh38.p7 | 17:9622417 | AAATAAACTGGACAT[A/G]TTGGTGGCACTGCCT | 146845 |
| rs552268934 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CFAP52 | GRCh38.p7 | 17:9579693 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 146845 |
| rs552319777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9641140 | TTAGGCACCTGTCTC[C/T]CCATCCCTAAGGTAG | 146845 |
| rs552346759 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9595829 | GTCCCCATGAGATGT[C/T]CTGCAAGTTTAAGTA | 146845 |
| rs552413253 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9599202 | CTGAAAATTCAAAAT[C/T]TGAGATGTGCTAATG | 146845 |
| rs552423043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9597664 | AGAAATTAGCTGGGC[A/G]TGGTGGCGGGCACCT | 146845 |
| rs552437007 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9627157 | AAAGAAGGGTTTTGG[A/G]TTATCTGCAAACTTG | 146845 |
| rs552458559 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633972 | AGGCGTGAGCCACCG[C/T]GCCTGGCCCATCTTA | 146845 |
| rs552524582 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9625206 | AAAAAAATCAATTAA[A/G]AAAAAAACACAGTAG | 146845 |
| rs552548866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9605098 | CACTCCTTGCTATTT[A/G]CCCAAAGGAGCTGAA | 146845 |
| rs552599279 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9641324 | GCCCAGTCTCTAGAA[A/C]TCTGGGGAGTGGGGA | 146845 |
| rs552629058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9590292 | GCCAAGGTGTTTTCC[C/T]ATCATCCAGCCAGGG | 146845 |
| rs552685356 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9591927 | TTCCGGCCATGGCTT[A/T]TAAAGAAACTGTGCT | 146845 |
| rs552806570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9589728 | CAAGAGCGAGACTCC[A/G]TCTCAAAAAAAAAAA | 146845 |
| rs552835578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598037 | TCAAGCTCCGCACTT[C/T]CTAATTTGGGAGGGG | 146845 |
| rs552855746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9630029 | GGCTCAGGACAGAAA[C/T]CTTGGAGTCCTCACT | 146845 |
| rs552934451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598527 | AGCATTTTGGGAGGC[A/G]GAGGTGGGTGAATCA | 146845 |
| rs552983462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9635276 | CACACCCCACCCAAC[C/T]GAGACAAAGACAGGG | 146845 |
| rs553004947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9635707 | AGAAGCCGTTCATGA[C/T]GGTCCATGGTTTATC | 146845 |
| rs553015021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9589402 | TTCACAAGTGGTCAC[C/T]CCTTCCCTGGCTCAT | 146845 |
| rs553064679 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9634038 | TTAAATACACCCAGA[C/T]GTTTTGACCATTATT | 146845 |
| rs553102809 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9622519 | GCATGCCAGCCTGGG[A/T]GACAGAGTAAGACCC | 146845 |
| rs553132892 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9625592 | ATTGTTAGCTGGTAA[C/T]GCTATGGTTTTTCTG | 146845 |
| rs553157690 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | CFAP52 | GRCh38.p7 | 17:9630574 | AGCTGGGACTACAGG[C/T]GCCCGCTACCACGCC | 146845 |
| rs553267406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9591277 | TCCCAACCTCAGGTG[A/G]TCCACCCTCCTCGGC | 146845 |
| rs553365339 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9579326 | GGGTTACAGCAATAG[A/C]GGGGGGCAGAGGAGG | 146845 |
| rs553459837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585153 | ATTACGAGAATTGGC[C/T]GTAGGACTTGCTGGA | 146845 |
| rs553473482 | in-del | -/TT | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9578307 | GGACATGACGGCACG[-/TT]TTAAGTGGGAAGCCT | 146845 |
| rs553489084 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9578324 | TAAGTGGGAAGCCTC[A/T]GTAAACTGGCCAGAG | 146845 |
| rs553514049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9640155 | ACACAGCACGTTTCC[A/G]ACATGAAACAATGAG | 146845 |
| rs553559565 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9625959 | TATGTGATGATACTC[C/T]TTCCTGCTTTCCTGT | 146845 |
| rs553569487 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9578145 | TTCAACAGGTTATAG[A/G]AGGAGCTATGAATAC | 146845 |
| rs553634240 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9589483 | CACGCCTGAAATCCC[A/T]GCACTTTGGGAGGCC | 146845 |
| rs553650269 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9617662 | TCTCTCGGCAGAAAC[C/T]CTACAAGCCAGAAGA | 146845 |
| rs553689796 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9595183 | TAGAAATCCTTTTTT[A/T]ATGTTATATACCAGT | 146845 |
| rs553748132 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9584691 | CAATAGTGTGATCTC[A/G]GCTCACTGCAACCTC | 146845 |
| rs553751431 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9603253 | TCGCTCTGTCGCCCA[A/G]GCTGGAGTGCAGTGG | 146845 |
| rs553758388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9615398 | CTTTATTTTCAACCT[A/G]TTAGTGTTTAGTTTT | 146845 |
| rs553892961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9614733 | GATGCTATTCTGTGC[A/G]TTAAAGGATGTTTGG | 146845 |
| rs553925652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9637293 | TATAGAACTAGAAGG[A/G]CATGTCTGAACTTAT | 146845 |
| rs553981846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9639416 | AGTCTGGGTGACAGA[A/G]CAAGACTCTCTCTTA | 146845 |
| rs554014430 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9600886 | TCTATGCCCTCGTCT[C/T]TGGTTTTTATTCTGG | 146845 |
| rs554147325 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9593432 | GCAGTCTCTGTTTTA[A/G]TAATTCTTTTGTTTG | 146845 |
| rs554177433 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9635104 | TTCACTTGGTTTTGC[A/G]TTGGCCCTTGCATTA | 146845 |
| rs554211524 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9593487 | TCGAGACGCAGTCTC[A/G]CTCTCTTGCCCAGGC | 146845 |
| rs554338944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9578663 | CTATTCTCCTGCCTC[A/G]GCCTCCAGAGTAGCT | 146845 |
| rs554418974 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9611302 | AGAAATCTGAAATGT[A/G]GAAGAGGAAAAACCA | 146845 |
| rs554519502 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638001 | GGACTTCTTACCATA[A/T]GCAGACAAGGGTTGA | 146845 |
| rs554527643 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9613674 | AGGCATGCACCACCA[C/T]GCCCGGCTAATTTTT | 146845 |
| rs554529281 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9585395 | AAGTGTTGGCCGGGC[A/G]CGGTGGCTCACACCT | 146845 |
| rs554582787 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638512 | ATGGAGATAAACCAA[A/C]CCAAATCCCAGCTTG | 146845 |
| rs554608774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9597117 | TCTACTGTCTCATGC[A/G]TTAGGCTTTTTTACA | 146845 |
| rs554669598 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CFAP52 | GRCh38.p7 | 17:9595016 | CTGCCTCAGCCTCCC[A/G]AGTACCTGGGATTAC | 146845 |
| rs554714261 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632462 | CCACACTGATCCCTG[A/C]ATAAATAAGTGGTTG | 146845 |
| rs554832443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9595927 | CAGTACGTTTAAAAT[A/G]TGTCTGAGTACTTAC | 146845 |
| rs554843674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9640568 | TGTCCCGGCAAAGGA[C/T]ATGATCTTGTTCCTT | 146845 |
| rs554843979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9634296 | GCACTATAAGAAGGC[A/G]TAAGCATCTGACTAC | 146845 |
| rs554902386 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9628244 | CTGTAAGACAATCAT[A/C]AAGGCTTCAGATAAT | 146845 |
| rs555011538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9593383 | AATTCTCAGATCCCA[C/T]GTACTGAATCAGAAA | 146845 |
| rs555027007 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9601425 | ATAATAATAAAATTT[A/T]AAAAAAAGTACCACA | 146845 |
| rs555071810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9587456 | CCACCCTGCTTTCCA[C/T]AATGGTTCAACTAAT | 146845 |
| rs555082102 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9600634 | CAGTGGCGAGATGTC[A/G]GTTCACAGCAAGCTC | 146845 |
| rs555096064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9607018 | CATTAAGACACAAAC[C/T]TATACAGTCACTAGC | 146845 |
| rs555193686 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584865 | TGACCTCAGGTGATC[C/T]GCCTGCCTCGGCCTC | 146845 |
| rs555288875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600878 | GCCAGTTCTCTATGC[C/T]CTCGTCTCTGGTTTT | 146845 |
| rs555310989 | in-del | -/TT | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9627126 | CCTTTTTTTTTTTTT[-/TT]GAGCTTGACAGACAA | 146845 |
| rs555330777 | snp | C/T | 0.00354629 | 0.0419591 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584392 | CACTCAGAACTGAAA[C/T]CGAAAGTTAAAAAAA | 146845 |
| rs555334094 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9582524 | TTTCCTTATTGCCTT[G/T]TAGGAGTTCTTCGTA | 146845 |
| rs555502406 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CFAP52 | GRCh38.p7 | 17:9637071 | CAAACAAACAAAAAA[A/G]CAAAAAAAAACCCGA | 146845 |
| rs555547286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9592849 | ATTTTGTGTGGACAT[A/G]TCTTCATTTCTCTTG | 146845 |
| rs555552113 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9574669 | TCTCCCGAGTAGCTG[G/T]GATTACAGGCATGTA | 146845 |
| rs555684673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9592200 | AGGCACGGTGGCTCA[C/T]GCCTGTATTCCCAGC | 146845 |
| rs555764315 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CFAP52 | GRCh38.p7 | 17:9599672 | ATGGGGTGCCAGAGG[A/G]ACCTCATCCCATTCC | 146845 |
| rs555811535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9582685 | TCTGTCACCCAGGCT[A/G]GAGTGCAGTGGCACA | 146845 |
| rs555833186 | in-del | -/AAAC | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9578111 | AATAAATAAATAAAT[-/AAAC]AAACAAACATACATA | 146845 |
| rs555839889 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575144 | TTTCATCATGCAGTC[C/T]TTGGGATTAACTGCT | 146845 |
| rs555872804 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP52 | GRCh38.p7 | 17:9583419 | TTTAAGAACAAGAAG[A/G]TTATATTAATAAATA | 146845 |
| rs555887882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9611856 | ATCATTTAACTATTC[C/T]ATTACAACTGGGTAT | 146845 |
| rs555923244 | in-del | -/T | 0.0879971 | 0.190408 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633676 | AATTGTCATCTTATC[-/T]TTTTTTTTTTTTTTT | 146845 |
| rs555981961 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9606081 | GCTCTAAAAAAAATA[A/G]CCTAGTAAAAACAAA | 146845 |
| rs556001375 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CFAP52 | GRCh38.p7 | 17:9606078 | ACTGCTCTAAAAAAA[A/T]TAGCCTAGTAAAAAC | 146845 |
| rs556034766 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9636803 | TGTAACCCCAGCACT[A/T]TGGGAGGCCGAGGTG | 146845 |
| rs556095725 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9626709 | GTTGACTTGATTTAC[A/G]TTAATCAAGACTGTC | 146845 |
| rs556108566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642105 | GCTATTTTTGGTGGG[C/T]ATTGATAATAGAAAT | 146845 |
| rs556135584 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9592358 | CCTGTAACCCCAGCT[A/G]CTAGGGAGGCTGAGG | 146845 |
| rs556259367 | in-del | -/TGATAT | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9614494 | CAATTTTACTTAGTC[-/TGATAT]TAAGATTACCACATC | 146845 |
| rs556371694 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9622506 | CAATCACACCAGTGC[A/G]TGCCAGCCTGGGTGA | 146845 |
| rs556561741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9592996 | GTCCCACTGTGGAAA[A/G]GGGAGAATTTATGGC | 146845 |
| rs556590692 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, missense, nc-transcript-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575802 | CTCACCAGGGGTCCG[A/G]TGCCATCCTGCAGAC | 146845 |
| rs556615512 | snp | C/T | 1.64855e-05 | 0.00287097 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600230 | TTTTTCTCCCTTCAC[C/T]GGCAGCATGTACTTT | 146845 |
| rs556618650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9606742 | CTTGCATCCCCAAGT[C/T]CCCAGATAAATGCTA | 146845 |
| rs556763810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598612 | ACTAAAAATACACAA[A/G]TAGCCAGGTGTGGTG | 146845 |
| rs556796232 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9641409 | AGCTTAGCTGTGGAT[A/G]CAGAGGCTGTTCTTT | 146845 |
| rs556840697 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9631844 | GTGATCTCGGTTCAC[A/T]GCAACCTCCGCCTCC | 146845 |
| rs556846062 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CFAP52 | GRCh38.p7 | 17:9630646 | CGTGTTAGCCAGGAT[A/G]GTCTGGATCTCCTGA | 146845 |
| rs556849423 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9624114 | TTTCAATATTTTTTC[C/T]TTGCTTTTGTCTTTC | 146845 |
| rs556919328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9579799 | TCTTGAACTCCTGAC[C/T]TCAGGTGATCCACCC | 146845 |
| rs557003534 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586062 | TGTTAGTTCTATGTG[A/G]CAATGTGCTTTATTC | 146845 |
| rs557047446 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | CFAP52 | GRCh38.p7 | 17:9629475 | CTTTTCTTTCTTTCC[C/T]TTTCTTTCTTTCTTT | 146845 |
| rs557065870 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9599439 | GGCACACCTTTATCC[A/T]AGGAGCCCTTAAGAG | 146845 |
| rs557093072 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9611656 | CAGGCATGAACAACT[A/G]TACAAGCTCTGAAAT | 146845 |
| rs557112374 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9622572 | AGAAGAAGAAGAAGA[A/T]GATGATGATGATGAT | 146845 |
| rs557155982 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9624925 | CTGTGTGCTTGCATT[A/T]TGTAGCAGTCAACCA | 146845 |
| rs557156415 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CFAP52 | GRCh38.p7 | 17:9604803 | AATAAATAAATAAAT[A/G]AAAGAAGATATACAG | 146845 |
| rs557232028 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9611016 | AACTGAGGCCAGAGG[C/T]TTCTGACAACTTGTC | 146845 |
| rs557297453 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CFAP52 | GRCh38.p7 | 17:9630681 | GTGATCCGCCCGCCT[C/T]GGTCTCCCAAAGTGC | 146845 |
| rs557324616 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9581222 | CTCGGGAGGCTGAGG[C/G]AGGAGAATGGCGTGA | 146845 |
| rs557360816 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9631200 | CACCTACAAGGCTCC[A/T]TGTGAATTTCTGTCC | 146845 |
| rs557395114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9590527 | GTTCCAACATCCTTC[A/G]TTCAACTTAAAGCAG | 146845 |
| rs557416753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9592147 | TCCACAATTTTAGAA[C/T]GTTTTCAACACCCCA | 146845 |
| rs557472970 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9579367 | AGTGCAGGGCCTGGT[G/T]GCAGAACGGCAAATA | 146845 |
| rs557486040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9625882 | TGCTTATACTTTTGA[A/G]CCCAGTTTTTCTCTA | 146845 |
| rs557493645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9635009 | TGTGAAAGTTTAAAT[A/G]TAGCTCTGGGTACTC | 146845 |
| rs557629966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9623080 | AATGTAGAGTTCCAC[C/T]TTTATTTCTCACAGT | 146845 |
| rs557686225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9606244 | TAAAAATTAGCCGGC[A/G]TGGTGGCATGCATCT | 146845 |
| rs557715819 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9626216 | ATAGGCCATCAAGTG[C/T]AGAGAGTTTGGAAGA | 146845 |
| rs557745934 | snp | A/G | 1.6495e-05 | 0.0028718 | missense | CFAP52 | GRCh38.p7 | 17:9586759 | GGCTGTCCCTTCACA[A/G]AGGCAAAATTGAAGC | 146845 |
| rs557746056 | in-del | -/TAAT | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584524 | TGTCTACGATCAAAC[-/TAAT]TAACATATTCACTTC | 146845 |
| rs557782108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9579821 | GATCCACCCGCCTCG[A/G]CCTCCCAAAGTGCTG | 146845 |
| rs557874685 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9593175 | CTTTTTCTTTAAACA[C/T]CTTGATTCGAACATT | 146845 |
| rs557883312 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP52 | GRCh38.p7 | 17:9611779 | ATGGTAACATATACA[C/T]GTACTACATAATCTT | 146845 |
| rs557952036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9599542 | CAGGCTAATTGGGGT[C/T]GAATATTTCCTCCCA | 146845 |
| rs557961379 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576492 | CAGAGAAATAGCACA[A/C]AAAAAAAGAAGAGGA | 146845 |
| rs558103572 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9626310 | TCTCAGCTCACTGCA[A/G]CCTCCGCCTCCTGGG | 146845 |
| rs558114060 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642044 | AAACATTTGCACAAG[A/C]GCCTTAAGAGCACAA | 146845 |
| rs558121418 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9630229 | ACCCAGTATACTTTC[C/T]CGCAGTCTGTTTTCG | 146845 |
| rs558146708 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9604862 | CTATGTCTTATATCA[G/T]CCGGGAAATGTAATT | 146845 |
| rs558193967 | in-del | -/T | 0.0652144 | 0.168387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633844 | ACCACGCCCAGCTAA[-/T]TTTTTTTTGTATTTT | 146845 |
| rs558250038 | snp | G/T | | | missense | CFAP52 | GRCh38.p7 | 17:9635411 | GGCTTTCAGGTGAGG[G/T]TATGGCAGATAGGCT | 146845 |
| rs558276648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9629914 | CTTTTCTTGGCCCTG[C/T]CTTCTCCTCCTTGTT | 146845 |
| rs558365436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9610172 | CATCCAAGTATTGTC[A/G]ATAATACAAGATGCA | 146845 |
| rs558383072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9605836 | GTAAATATATGTTGC[C/T]ATTAATTTGTCCAAA | 146845 |
| rs558413904 | snp | A/G | 0.000148303 | 0.00860985 | missense | CFAP52 | GRCh38.p7 | 17:9594248 | GGCAGCCCTGCAGCC[A/G]GCCTCAATGTTGGCA | 146845 |
| rs558452616 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9611610 | CCTCAAGTGGTCCTC[C/T]TTGCCTAGGCCATCC | 146845 |
| rs558468415 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9620176 | ATACAAAATCAATGT[A/G]CAAAAATCACAAGCA | 146845 |
| rs558607927 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9597374 | ACAATTTTAAGTATT[C/G]TCACCGCCAAAAAAA | 146845 |
| rs558625860 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9590723 | AGGTTAATCTGGCAA[A/T]ACTGTTAATCTCTGC | 146845 |
| rs558660523 | snp | A/T | 0 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9639246 | ACCAGCCTAGCCAAC[A/T]TGGTGAAACCCCATC | 146845 |
| rs558671500 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9595541 | TTGACTAAGCCAGGG[C/T]TTTATAGGGTTCTTT | 146845 |
| rs558689071 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9589263 | ATGTATATTTTCTTA[C/T]TTAAGCTTCATAGGT | 146845 |
| rs558747526 | snp | A/G | 3.32016e-05 | 0.00407427 | intron-variant | CFAP52 | GRCh38.p7 | 17:9635578 | ACCTGTGATGGGGAG[A/G]ATGCAGTGATACCTG | 146845 |
| rs558788029 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9586034 | TCCCTAGAAGAACTG[C/T]CCCACTTCAAGTTGT | 146845 |
| rs558812431 | in-del | -/TTTTG | 0.00478085 | 0.0486577 | intron-variant | CFAP52 | GRCh38.p7 | 17:9623670 | ACTTTGCTTAGCTTT[-/TTTTG]TTTGTTTGTTTGTTT | 146845 |
| rs558818102 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9629675 | GTCTCAGCCTCCAGA[A/G]TAGCTGGGATTACAG | 146845 |
| rs558819546 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9574722 | TATTTTTAGTAGAGA[C/T]GGGGTTTCTCCATGT | 146845 |
| rs558856695 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9610013 | AGAGAGAGAGAGAGA[C/G]AGAGACAGAGAGAGA | 146845 |
| rs558874439 | in-del | -/GACAT | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9581836 | TGGCTCAGCCAATCA[-/GACAT]TCCCACTCCGCAGTT | 146845 |
| rs558877665 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9597995 | AGAGTGAGACGGAGC[C/G]AGGTGTGAATCCCTG | 146845 |
| rs558919557 | snp | A/G | 0.130008 | 0.219321 | intron-variant | CFAP52 | GRCh38.p7 | 17:9620861 | ATCAATTCAAGATGG[A/G]TTAAAGATTTAAACG | 146845 |
| rs558975037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9639842 | ATCTCTGGCAGAGGA[C/T]ACTCCAGTAAGATGG | 146845 |
| rs559002685 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584539 | TAATTAACATATTCA[C/T]TTCACATAGTTACTT | 146845 |
| rs559036067 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP52 | GRCh38.p7 | 17:9640380 | AGCTATTCTTCCTGA[C/T]GCTCTTCCTCCCCCC | 146845 |
| rs559057328 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9588645 | CTTGTTTCAGGTCTT[A/C]GTGGAAAGGCTTTCA | 146845 |
| rs559064204 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9582434 | CTTTTTGTAGGTTTA[C/T]TGGGTTTTGAATTTC | 146845 |
| rs559078108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9616141 | AGGCCAGTGTGTGCG[C/T]GCACCGTGCGCGAGC | 146845 |
| rs559089696 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585498 | ATGGTGAAACCCCGT[A/C]TCTACTAAAAATACA | 146845 |
| rs559102907 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9622310 | CACAGCACTTTGGGA[G/T]ACTGAGGTGGGAGGA | 146845 |
| rs559265859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584984 | TTTGTAAAGACATGG[A/G]TTAACCTGGAGAATA | 146845 |
| rs559333062 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9578709 | CACCACCACGCCTGG[C/G]TAATTTTTGTATTCT | 146845 |
| rs559345009 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9579516 | TTAGAAACAAAAGCA[A/C]GGCCCCTTTTTTCAC | 146845 |
| rs559346302 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9616164 | GCGCGAGCCGAAGCA[A/G]GTCGAGGCATTGCCT | 146845 |
| rs559392695 | in-del | -/GGTTACAATTTCCA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9635738 | GATGCTAGTGGGGAG[-/GGTTACAATTTCCA]GGAAGAACTGAATGT | 146845 |
| rs559420950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9627641 | TCGACTTATCTTCAA[A/G]CTCAGGTAATATACA | 146845 |
| rs559422435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633932 | GTGATCCGCCTGCCT[C/T]GGCCTCCCAAAGTGC | 146845 |
| rs559552359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9622733 | ATATATGCAAAATAC[A/G]TAAATCATAAATAAG | 146845 |
| rs559552738 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584618 | GCAGTATTTTTTTTT[A/T]AATTTATTTGTTCAT | 146845 |
| rs559599635 | snp | A/C | 0.0298908 | 0.118541 | intron-variant | CFAP52 | GRCh38.p7 | 17:9629713 | CCTGCCTCAGCCTCC[A/C]AAGTATCTGGGACTA | 146845 |
| rs559614045 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9611206 | AACTAAACTAGTTAC[A/C]GAGAGAGTCTGTATC | 146845 |
| rs559639293 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9578485 | CAGTTGTTTTCATAT[A/T]GCTTATCTCAAGATA | 146845 |
| rs559647033 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9579924 | TACTTGACACTTGTA[G/T]GTATTGCATTTTGGC | 146845 |
| rs559729012 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9638921 | GTACCACTGACCTCA[C/T]AGAGTAAGGATTAAA | 146845 |
| rs559734120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9593838 | GACATGGTGGTGTGC[A/G]TCTGTAGTCCCAGCT | 146845 |
| rs559905341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9601520 | GCCCCATTGCCATAC[A/G]TAAGAGAAGTGTGCT | 146845 |
| rs559912254 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9637356 | TTAAAGCTGTTCCGT[G/T]GTGTAGCAGGAATTC | 146845 |
| rs559991884 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9594414 | CTGGGGGAACACGTC[G/T]TTAGTCCTGGATAAA | 146845 |
| rs560084144 | in-del | -/T | 0.324619 | 0.238604 | intron-variant | CFAP52 | GRCh38.p7 | 17:9630427 | AGCTAATTTTTGTAA[-/T]TTTTTTTTTTTTTTT | 146845 |
| rs560168977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9607866 | GCACTGAATCCCCTT[A/G]GTCAGCCTGGGGGTG | 146845 |
| rs560179165 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB, intron-variant | CFAP52, USP43 | GRCh38.p7 | 17:9643718 | TGTGAGAATTAAGTG[A/G]CTAATGTACTAAAGC | 146845 |
| rs560185324 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585477 | TTCAAGACCAGCCTG[A/G]CCAACATGGTGAAAC | 146845 |
| rs560269605 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632673 | ATTGAGGGTAATCAA[C/G]GAAGACTCAGGCTGT | 146845 |
| rs560298006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9583991 | GACCACCTCACCGAG[C/T]TGAGTCTCTGAATCA | 146845 |
| rs560310018 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9594776 | GATCAGCTTTAACCA[A/G]CTAATGGTGACCTAG | 146845 |
| rs560405723 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9636644 | CTATATCACTGCATA[C/G]GAGAGACGAGGATAA | 146845 |
| rs560419995 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9599775 | AGACAGAGTTTTGCT[C/G]TTGTTGCCCAGGCTG | 146845 |
| rs560420735 | snp | G/T | 0.000810509 | 0.0201146 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598222 | GGTTTTTTGTTTTTT[G/T]TTTTTACATAGTGGG | 146845 |
| rs560421948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586407 | CATCTCTACTAAAAA[C/T]ACAAAATTAGCAGGG | 146845 |
| rs560545947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600302 | CCTGGAGTACAGTGA[C/T]GTGATCTTGGCTCAC | 146845 |
| rs560554556 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CFAP52 | GRCh38.p7 | 17:9627034 | TTGTACCCCAATATT[A/C]CTTCTTCTTATTATT | 146845 |
| rs560574087 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9631459 | CTGCTAAGGTCAAGA[C/G]GTGACATTAAAGCTT | 146845 |
| rs560625015 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632025 | TGATCCGCCTGCCTT[A/G]GCCTCCCAAAGCGCT | 146845 |
| rs560631904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9613678 | ATGCACCACCACGCC[C/T]GGCTAATTTTTTATA | 146845 |
| rs560633796 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9626240 | TGGAAGAAAGTTCTT[C/T]TTTTTTGAGATGGAG | 146845 |
| rs560647613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9582793 | AGGTGTCCACCACTA[C/T]GCCCAGCTAATTTTT | 146845 |
| rs560655345 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9625070 | GGTTCAGCTTCCTGC[C/T]ATCCAAGCTGAGCTC | 146845 |
| rs560679111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9602237 | ACCCATTAACCCGTC[A/G]TCTACATTAAGTATT | 146845 |
| rs560692915 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9614254 | TCTGCCTCCCAGGTT[A/C]AAGCAATTCTCCCAC | 146845 |
| rs560822901 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9581974 | CCCATTTTTCAAGTG[C/T]GACCCAAACTTCCTG | 146845 |
| rs560840052 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9640143 | AGAGTGACTGGAACA[C/T]AGCACGTTTCCGACA | 146845 |
| rs560894261 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9589470 | GGGTGTGGCAGCTCA[C/T]GCCTGAAATCCCAGC | 146845 |
| rs560903712 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9596669 | CAACTCAATACCTTG[-/A]AAAAAACACATTTAA | 146845 |
| rs560962989 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9608631 | GCATTGTGTTAATCA[G/T]GCATTTGAATACAAT | 146845 |
| rs560970743 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9628441 | TGCACCACCATACCC[A/G]GCTAATTTTTGTATT | 146845 |
| rs560999210 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B | CFAP52, USP43 | GRCh38.p7 | 17:9643400 | GAATAATTTGTGCAG[A/G]CTCTAATTAGAACTT | 146845 |
| rs561001304 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CFAP52 | GRCh38.p7 | 17:9636960 | TGAGGCAGGAGAATC[A/G]CTTGAACCCGGGAGG | 146845 |
| rs561047429 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633807 | TCAGCCTCCTGAGTA[G/T]CTGGGACTACAGGTG | 146845 |
| rs561056366 | snp | A/T | | | missense | CFAP52 | GRCh38.p7 | 17:9638624 | GCGTCTCAGGAGGAA[A/T]CAGATGATACTAGCC | 146845 |
| rs561172375 | snp | A/G | | | missense, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643118 | ATCACACGCATCCGC[A/G]TAAGTCCAGGAAATC | 146845 |
| rs561180773 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9615866 | GCTGGTTTTCAACTG[A/C]CATCCTCAAGCAATC | 146845 |
| rs561183167 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9639530 | TTCACCCTTGGAGCA[A/T]GCAAGGGGTCCCTGC | 146845 |
| rs561187444 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633215 | TTATAAATGTATACT[A/T]ATTTTGAAATGGAGT | 146845 |
| rs561206001 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9593675 | TGGCCAGGTTGGTCT[C/G]AAACTCCTGACCTCA | 146845 |
| rs561247141 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9631563 | CCTCAGGAGGGAGAT[C/T]GCTTGGTGGATTTGA | 146845 |
| rs561285328 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9605010 | GAATGCAAAATAGTA[C/T]GGCCACTTTGGAAGA | 146845 |
| rs561320642 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632070 | GAGCCACTGCGCCCA[G/T]CCTCCACTTTTTTTT | 146845 |
| rs561348236 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9629950 | CCCTACCCCACCCTG[C/G]GCATGTCTTCTCCAC | 146845 |
| rs561470784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9577799 | CCACACACATAGAAC[C/T]CTGCAACTGAGGCCG | 146845 |
| rs561503102 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9603502 | GCGTGAGCCACCACA[A/C]CCGGCCCTAAGTAGA | 146845 |
| rs561538135 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642880 | AATTTACTGCAACAG[A/G]TAGATTTTTATAATC | 146845 |
| rs561564355 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9605881 | AATGCCAAGAGGGAA[C/T]CCTAATGTACACAAT | 146845 |
| rs561579279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9614312 | AGGCATGTGCCACCG[C/T]GCCCAGCTAATTTTT | 146845 |
| rs561585643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576973 | TCCAAGCCTCAGGGA[A/G]TGAGATGGTTTTTAC | 146845 |
| rs561646166 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9606371 | CTGGGTGGCAGAGAC[A/C]CTGTCTCCAAAATAC | 146845 |
| rs561748410 | in-del | -/AAAC | 0.0134861 | 0.0810011 | intron-variant | CFAP52 | GRCh38.p7 | 17:9610206 | ATAAAATCAAGTAAA[-/AAAC]AAACAAACTATGTTG | 146845 |
| rs561763651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9591140 | CCTCCCAGGTTCAAG[C/T]GATTCTCCTGCCTCA | 146845 |
| rs561830211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600001 | CCGCCTCGGCCTCCC[A/G]AAGTGCTGATATTAC | 146845 |
| rs561867764 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575670 | AGTAAAGGAAAGGTC[C/T]CGCTGCCCCTCCCCT | 146845 |
| rs561888189 | snp | A/T | 0.000399281 | 0.0141238 | stop-gained | CFAP52 | GRCh38.p7 | 17:9598308 | GCCAAACAGGACAGT[A/T]GAAAAGAATAGTCAT | 146845 |
| rs561939136 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9593086 | CCAATGTGATAATAC[A/T]TTCCATATGTAGAAA | 146845 |
| rs561949550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586330 | GCACTTTGGGAGGCC[C/T]AGACGGTCGGATCCC | 146845 |
| rs562032417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9604390 | CCTGAATAAGGACTG[C/T]TACCCAAAATATACA | 146845 |
| rs562063221 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9635577 | TACCTGTGATGGGGA[A/G]GATGCAGTGATACCT | 146845 |
| rs562065794 | in-del | -/AAAA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636179 | AACTCTGTCTCAAAA[-/AAAA]GAAAGAAAGAAAGAA | 146845 |
| rs562099546 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9632151 | GGCGGACTCTTGGCT[C/T]ACTGCAACCTCCATC | 146845 |
| rs562129781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598901 | CGAAAGCCTGCCTCA[C/T]CTGGATGAAAGCAAT | 146845 |
| rs562148830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9580972 | TGATATTGTCTATAA[C/T]AGCTGAAACATTGGA | 146845 |
| rs562217995 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584632 | TAATTTATTTGTTCA[-/T]TTTTTTGAGATGGAA | 146845 |
| rs562254713 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9628482 | ACGGGGTTTCACCAT[A/G]TTGGTCAGGCTGGTC | 146845 |
| rs562316720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9614068 | GGTAGATTTTAAACC[A/G]TCTTTTCAATTGCTT | 146845 |
| rs562321399 | snp | C/T | 0.000105716 | 0.00726957 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641703 | CTGAGTCCTGCTTAA[C/T]GCTTCTTTCCTGAAT | 146845 |
| rs562356476 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9630726 | TGAGCCACTGCGCCC[G/T]GCCCGATTTTTGTAA | 146845 |
| rs562481656 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9637427 | GTTTGAAAACTTCCA[C/T]AATGAGAAGAAACTG | 146845 |
| rs562573152 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9612174 | TGAGTAACTCCTGCC[G/T]TTTCAACTGTGTCAC | 146845 |
| rs562686662 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9637453 | AACTGTGCAGAAGGT[A/G]CATTTTTTAGCCAGG | 146845 |
| rs562701028 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9591595 | AACAAATTTGTGTTT[G/T]TGCGGGGTGCAGTGG | 146845 |
| rs562741834 | in-del | -/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9624696 | GCTTCTGACTCTGCC[-/T]TTTTTTTTGAGTCAT | 146845 |
| rs562749899 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9596193 | CAACCTCTGCCTCCC[A/G]GGTTCAAATGATTCT | 146845 |
| rs562751919 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9582077 | CTAGTTTGCAACCAA[G/T]AACCATAATTTTTAA | 146845 |
| rs562813196 | in-del | -/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631769 | AAATGTTTTGGAAAG[-/T]TTTTTTTTTTTTTTT | 146845 |
| rs562833603 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9599893 | ATTATAGGCATGCAC[C/G]ACGACACCCAGCTAA | 146845 |
| rs562854055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9626422 | TTTAGTAGATACAGC[A/G]TTTTGCCATGTTGGC | 146845 |
| rs562890689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9581517 | AGTGTACATATGTTT[A/G]AGAGAGAGAGAGGGG | 146845 |
| rs562924273 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP52 | GRCh38.p7 | 17:9592327 | AAAAATTAGCTGGGC[A/G]TGGTGGTGGTGGGCC | 146845 |
| rs563053687 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9631359 | AATATTCTTTCCCTA[G/T]ATACCTCCATGGCTC | 146845 |
| rs563061239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9635303 | AGGGAATTAAAAAAA[C/T]ACAAATCAAGCATAG | 146845 |
| rs563133573 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9639767 | TCCTTAAGGAGCAGC[A/C]TCTGAGTGAGGCCTG | 146845 |
| rs563142741 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9625186 | CTTTAGCAGTAGAAT[A/C]CTTAAAAAAAATCAA | 146845 |
| rs563181203 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9630777 | TTTCGCCTGAGGTCA[G/T]GAGTTTGAGAACAGC | 146845 |
| rs563181779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586345 | TAGACGGTCGGATCC[C/T]CTGAGGTCAGGAGTT | 146845 |
| rs563244974 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642322 | CTCTTTGATTCATCA[A/G]GATATTAACAAATAA | 146845 |
| rs563310105 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585688 | ACACACACACACACA[A/C]AAAGTGTTGTGTTTT | 146845 |
| rs563311748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9609601 | CTCAGGAGGCTGAAG[C/T]GGGAGGATTGATTGA | 146845 |
| rs563356215 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585514 | TCTACTAAAAATACA[A/C]AAAAAAATTAGCCAG | 146845 |
| rs563378077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9590952 | TTATTCTACCCAACC[C/T]ATCTAGCTTCTACAC | 146845 |
| rs563379569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9610427 | CCACCTGCTGGGCTT[C/T]TTGTAGATTGAAAAG | 146845 |
| rs563379665 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9603239 | TTTGATACAGAGTCT[C/T]GCTCTGTCGCCCAGG | 146845 |
| rs563420302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585700 | ACACAAAGTGTTGTG[C/T]TTTGTACTCAAGTAG | 146845 |
| rs563435753 | snp | A/G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9604539 | TTGGGAGGCTGAGGC[A/G/T]GGCCGATCACCTGAG | 146845 |
| rs563507601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9605027 | GCCACTTTGGAAGAT[A/G]GTTTGGTGGTTTCTT | 146845 |
| rs563517194 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9614431 | AAAGTGCTGGGATTA[C/T]AGGCGTGAGCCACCA | 146845 |
| rs563588454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9578863 | AGGGTGGAGGGGTGC[A/G]TGGCCTTAGGTCCTG | 146845 |
| rs563637762 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9616255 | ACGCACCTGGAAAAT[C/T]GGGTCACTCCCACCC | 146845 |
| rs563661467 | in-del | -/TAAA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9604802 | AAATAAATAAATAAA[-/TAAA]AGAAGATATACAGAT | 146845 |
| rs563673494 | snp | A/T | 0.0349115 | 0.127424 | intron-variant | CFAP52 | GRCh38.p7 | 17:9622012 | AGTATAATAAAAAAA[A/T]AAATAAATAAATATA | 146845 |
| rs563733904 | in-del | -/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9599745 | CAAGTTTTCTTCTTC[-/T]TTTTTTTTTTCCTGA | 146845 |
| rs563768751 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9624286 | TCACTTCTGTTCCCC[C/T]GAGATTTGAATTATC | 146845 |
| rs563785661 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9596555 | ATCAAGTCCTGTGTT[-/A]GATGCTAATTTGGTT | 146845 |
| rs563907216 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9590233 | TCTGGCAAAGGGCTA[C/T]ACCCTTTGGCTTACC | 146845 |
| rs564084550 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9574741 | GTTTCTCCATGTTGG[C/T]CAGGCTGGTCTCGAC | 146845 |
| rs564155822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9604235 | AAGATGTGGTGATAA[C/T]TTTTAGCTATAATAC | 146845 |
| rs564218151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9605129 | AACTTATGTTCACAC[A/G]AGAACCTGCACACAG | 146845 |
| rs564261230 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | CFAP52 | GRCh38.p7 | 17:9605746 | TTGCCATGGGTTAGC[A/G]GGGAGGGAGGAGTGA | 146845 |
| rs564286643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9599974 | TTGAACTCCTGACCT[C/T]AGGTGATCCACCCGC | 146845 |
| rs564342174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9591418 | TCATGTTGTAATGCA[A/G]CCTGCTTTTTGACTA | 146845 |
| rs564380365 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CFAP52 | GRCh38.p7 | 17:9629736 | TGGGACTACAGGCGT[A/G]TGTCATCACGATGGG | 146845 |
| rs564380645 | in-del | -/GAGA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636251 | AAAGAAAGAAAGAAA[-/GAGA]AAGAAAAATAACTAA | 146845 |
| rs564399873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9612604 | TTAAATTTTTCTAAC[A/G]TGGTGAATTATTTTA | 146845 |
| rs564415371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9610511 | TGGACAGCTCCAGTG[C/T]CAAGATCTTTCCTTT | 146845 |
| rs564451235 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CFAP52 | GRCh38.p7 | 17:9627375 | AATTAGCCAGACATG[A/G]TGGCACATGCCTGTA | 146845 |
| rs564458720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9611157 | CCATGCTGGCTTCTT[A/G]CACAAGAACCTGCGT | 146845 |
| rs564463323 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9627166 | TTTTGGGTTATCTGC[A/G]AACTTGAATTCTGGC | 146845 |
| rs564506943 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9635338 | GGGGAAAAAGCTCTT[G/T]GAATCTTTTCCTATC | 146845 |
| rs564574017 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631861 | CAACCTCCGCCTCCC[A/G]GGTTCAAGCGATTCT | 146845 |
| rs564717329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9583097 | GGAAGATATTGTTTG[C/T]GTAAGGTGTGAATTA | 146845 |
| rs564718221 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB, intron-variant | CFAP52, USP43 | GRCh38.p7 | 17:9643771 | TAGAGAGAAATATGC[A/G]TGCTTTCTCAAAGAA | 146845 |
| rs564751591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9579426 | GGCAGGATAACACAG[A/G]AAAGAGAAGCTGGAA | 146845 |
| rs564836641 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9607888 | CTGGGGGTGCATCGC[A/G]AGCAGAACCTTCATG | 146845 |
| rs564860142 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9589016 | CTGAGGCAGGAGAAT[C/G]ACTTGAACCTGGGAG | 146845 |
| rs564876472 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9585398 | TGTTGGCCGGGCGCG[A/G]TGGCTCACACCTGTA | 146845 |
| rs564915459 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633833 | AGGTGCCTGCCACCA[C/G]GCCCAGCTAATTTTT | 146845 |
| rs564959734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9622147 | TGTTGAAATTATTTG[A/G]AATTCTAGATCTTTG | 146845 |
| rs564969957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9595433 | CATGAAGCTAATTGA[C/T]CGGCACGAAAACCAG | 146845 |
| rs565019415 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585394 | AAAGTGTTGGCCGGG[C/T]GCGGTGGCTCACACC | 146845 |
| rs565039293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9629141 | ATGTGAGGACCCTTT[C/T]TGTTGTGTAAGAGAT | 146845 |
| rs565043039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632612 | AACAGTAAAGCTGGT[A/G]GAAATTGTTGATGGA | 146845 |
| rs565058842 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9616363 | ACGCCCACGGAATCT[C/G]GCTGATTGCTAGCAC | 146845 |
| rs565094017 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9633681 | TCATCTTATCTTTTT[C/T]TTTTTTTTTTAGACG | 146845 |
| rs565185628 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9634416 | TTGGGAGGCTGAGGC[A/C]GGTGGATCACCTGAG | 146845 |
| rs565290138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9608736 | ATTTAATTAAAATAA[A/G]ATGAAACAAAACCTT | 146845 |
| rs565309724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9614911 | CTTACTACTGATGCA[A/G]TTTTGTAATCAGAGC | 146845 |
| rs565404777 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9623537 | TTTTCAAGAAATTAA[C/G]AGAAGAAAAAATTTA | 146845 |
| rs565427140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9583963 | CAGGGGAGACAATAA[A/G]CTAGCGTTCAAAGAC | 146845 |
| rs565495363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9602345 | TGTCCTCATTGTTCA[A/G]CTCTCACTTATGAAT | 146845 |
| rs565534877 | in-del | -/CTTT | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9629495 | TTTCTTTCTTTCTTT[-/CTTT]TCTTTTCTTTCTTTC | 146845 |
| rs565571606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9607144 | TCAGGTGAGGAGTTC[A/G]AGACCAGCCTGGCCA | 146845 |
| rs565599325 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633380 | CAGCTAATTTTTCTA[A/T]TTTTAGTAGAGATGG | 146845 |
| rs565619668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584824 | GACCGGGTTTCACCA[C/T]GTTGGCCAGGCTGGT | 146845 |
| rs565658366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9628569 | GGTTTGAGCCACCGC[A/G]CCCAGCCTTTTCCTA | 146845 |
| rs565660195 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9628127 | CTTATTCTTTTTGAG[A/C]AACTTTGTCCCAACC | 146845 |
| rs565667199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9616006 | AGGAGCCAAGATGGC[C/T]GAATAGGAACAGCTC | 146845 |
| rs565669888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9578638 | GCAACCTCCACCTCC[C/T]GGATTCAAGCTATTC | 146845 |
| rs565726638 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9616413 | GCAAGGCGGCAACGA[C/G]GCTGGGGGAGGGGCG | 146845 |
| rs565756075 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9606514 | ATAAACGCCTAATGA[A/G]ATAGGTACCATTTTC | 146845 |
| rs565759766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9591593 | AAAACAAATTTGTGT[C/T]TGTGCGGGGTGCAGT | 146845 |
| rs566031480 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9601336 | TTAATGGGTGCAGCA[C/T]ACCAACATGGCACAT | 146845 |
| rs566059807 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638449 | GACCTGAAGTCTGTT[G/T]TGAAGAAATACAAGC | 146845 |
| rs566088087 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | CFAP52 | GRCh38.p7 | 17:9593279 | TGATTGCACCCAGAA[G/T]AAGGAAGTGTAACCC | 146845 |
| rs566094053 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9614409 | GATCCACCCGCCTTG[C/G]CCTCCCAAAGTGCTG | 146845 |
| rs566107551 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584788 | ACCAAGCCCAGCTAA[-/T]TTTTTTGTATTTTTA | 146845 |
| rs566220630 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9592807 | AAATTATTATTAATA[A/C]TGGCGCTATGAACAT | 146845 |
| rs566232240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9595472 | AGCAACCTAAAGCAA[C/T]TGACCACGGGCTGTG | 146845 |
| rs566295347 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CFAP52 | GRCh38.p7 | 17:9589071 | TGCACCACTGCACTC[C/T]AGCCTAGGTAACAGA | 146845 |
| rs566368750 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CFAP52 | GRCh38.p7 | 17:9594893 | AGCAAATTAGGGAGG[A/G]TTTTTTTTTTTTTTT | 146845 |
| rs566453861 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9625906 | TTCTCTACAGCTCTT[A/T]TCTGGCTGATTTCTA | 146845 |
| rs566538447 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642556 | TTGAGCCTGGGAGGC[A/G]GAGGCTGCAGTGAGC | 146845 |
| rs566549215 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575023 | CAAGAACGTTATAGA[C/G]CTGTAATATGTTTTT | 146845 |
| rs566597331 | snp | A/C/G | 9.88849e-05 | 0.00703091 | missense, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643110 | GTGGCAACATCACAC[A/C/G]CATCCGCATAAGTCC | 146845 |
| rs566644520 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9588263 | AAAGGGATAATTGCC[A/C]TGTGGACACTGTGCA | 146845 |
| rs566664800 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9598634 | GGTGTGGTGGTAGGT[A/G]CCTGTAATCCCAGCT | 146845 |
| rs566677704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632203 | CTACTTCAGCCTCCC[A/G]AGTAGCTAGGACTAA | 146845 |
| rs566693932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9583133 | CTAAGTTTAATTTTT[C/T]CATATGGATAGCCAT | 146845 |
| rs566710402 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9616004 | GGAGGAGCCAAGATG[A/G]CCGAATAGGAACAGC | 146845 |
| rs566737978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9582425 | GTTGCATCTCTTTTT[A/G]TAGGTTTATTGGGTT | 146845 |
| rs566754981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9581621 | AATGGAGTGTGTGTG[A/G]GTATGTCTGGAGAAG | 146845 |
| rs566756330 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9591821 | AGTTTGAGGCTGCAG[C/T]GAGTGGTGATCGTGC | 146845 |
| rs566805732 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576546 | TCCCCATACCCCTTC[A/G]TTTCCAAGAATGCTA | 146845 |
| rs566832265 | in-del | -/ATA | | | cds-indel, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643056 | TCAAAGTTTGGGATT[-/ATA]ATGAGGGTGAAGTGA | 146845 |
| rs566848567 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9623908 | ACTGAATAATTATCT[C/G]AGTTTTTATTTATCT | 146845 |
| rs566848647 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9630938 | TTGCAGTGAGCCAAG[A/T]TCGCACCACTGCACT | 146845 |
| rs566886695 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9613737 | TTGGCCAGGCTGGTC[C/T]TGAACTCCCGACTTC | 146845 |
| rs566909892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9624778 | TATTATATAGAATAT[A/G]CTATAGCAACTCTGT | 146845 |
| rs566934810 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586202 | TGCTCACAAACAAAA[G/T]TTCCCGCTTAAAGCT | 146845 |
| rs566943863 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9583334 | AGCAAAAATAATCCA[G/T]TTAGCTACAGGAATC | 146845 |
| rs566970213 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9634203 | CTTTGAGATATTTTC[C/T]TTTCCTTTCCTTAAT | 146845 |
| rs566983160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9630492 | TGGAGTGCGGTGGCG[C/T]GATCTCGGCTCACTG | 146845 |
| rs566994853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9581177 | AAAAAATTAGCCGGG[C/T]GCGGTGGCGGGCACC | 146845 |
| rs567019245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9606026 | GGGGAAATCTCAAAT[A/G]CTTGTATCTTCTGTT | 146845 |
| rs567155882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9612890 | TTTTGTTTTTCCCTT[C/T]CAGTACAGTATTCAA | 146845 |
| rs567168929 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9608347 | ATCTTGCTGTTAGAA[G/T]GAGTAGTTGGAATCA | 146845 |
| rs567216280 | in-del | -/GAGGTTGCAGTGAGCC | 0.0310518 | 0.120672 | intron-variant | CFAP52 | GRCh38.p7 | 17:9592401 | TGAACCCAGGAGGCA[-/GAGGTTGCAGTGAGCC]GAGGTTGCAGTGAGC | 146845 |
| rs567217659 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB, intron-variant | CFAP52, USP43 | GRCh38.p7 | 17:9643777 | GAAATATGCATGCTT[C/T]CTCAAAGAAAATGTG | 146845 |
| rs567244620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9614645 | AAAAGGACTTCTGGG[A/G]AAAATTGAATTAGGC | 146845 |
| rs567247995 | snp | G/T | 0.0178098 | 0.0926698 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632253 | AGGCAAGTTTTTTTT[G/T]GTTTTTTTTTTTCAT | 146845 |
| rs567399834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9637724 | GGATTACAGGCATGC[A/G]CCACCACGCCTGGCT | 146845 |
| rs567470947 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9627042 | CAATATTACTTCTTC[G/T]TATTATTTGAATTGG | 146845 |
| rs567525160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632743 | GGGAAAGGGGCCTAT[A/G]GTGACCAGCATTCAG | 146845 |
| rs567544411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9577312 | GTTTCTAAATGATGA[A/G]GATTTCAGACCAGGA | 146845 |
| rs567570149 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576238 | ATGTAAATTATACCT[C/T]AACGCTTTTTAAAAA | 146845 |
| rs567622591 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9579769 | CACGGTGTTTCGCCA[C/T]GTTGGCCAGGCTGGT | 146845 |
| rs567708123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9606085 | TAAAAAAAATAGCCT[A/G]GTAAAAACAAAAATA | 146845 |
| rs567708215 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9613801 | TGGGATTACAGGCGT[A/G]AGCCACTGCACCCGG | 146845 |
| rs567710906 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | CFAP52 | GRCh38.p7 | 17:9631106 | AGAAAGAGAAAGAAA[A/G]AACATAAGTCAGAAT | 146845 |
| rs567768760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9624802 | ACTCTGTTCTCTGAG[A/G]ATTGTTGGCATGGAC | 146845 |
| rs567779012 | snp | A/C | 0.000107741 | 0.00733887 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575782 | ACCGCCGCCCTCACC[A/C]GGGACTCACCAGGGG | 146845 |
| rs567794271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9601099 | AAAAAAGGATGAGTT[C/T]ATGTCCTTTGTAGGG | 146845 |
| rs567816231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600625 | GCTGGCGTGCAGTGG[C/T]GAGATGTCGGTTCAC | 146845 |
| rs567933232 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598579 | CCAGCCTGGCCAACA[G/T]GGTGAAACCTTGTCT | 146845 |
| rs567979763 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9580966 | TCACTGTGATATTGT[A/C]TATAATAGCTGAAAC | 146845 |
| rs568042873 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9636185 | GTCTCAAAAAAAAGA[A/G]AGAAAGAAAGAAAGA | 146845 |
| rs568074908 | snp | C/T | 0 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9604706 | CCGGCAGTGAGATCA[C/T]GCCATTGCACTTCAG | 146845 |
| rs568080111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9599268 | ATTTCCGATTTTGGA[A/G]CATTTCAGATTTTAG | 146845 |
| rs568181622 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9581206 | CCTGTAGTCCCAGCT[A/T]CTCGGGAGGCTGAGG | 146845 |
| rs568209164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9589838 | GAAAAAGCCTTGTTT[C/T]ATTTTAATGACTGAT | 146845 |
| rs568301293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9623061 | GTTAAGGTCTCAGGC[A/G]ATGAATGTAGAGTTC | 146845 |
| rs568389058 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9619390 | AAAGAGTCCGGGACC[A/T]GATGGATTCACAGCC | 146845 |
| rs568395265 | snp | A/G | 1.64746e-05 | 0.00287002 | intron-variant, missense | CFAP52 | GRCh38.p7 | 17:9585875 | ATACTAAAGAGCAGA[A/G]CTTCCTACAGGGTCA | 146845 |
| rs568438299 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9622545 | GACCCTGTTTCTATT[A/T]AAAAAAAAAGAAGAA | 146845 |
| rs568503325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9596826 | GTACAAGCGATTCTC[C/T]TGCCTCAGCCTCCCG | 146845 |
| rs568619884 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9605967 | CTCTGCTGGAAGATA[C/T]TGATAATGGGAGAGG | 146845 |
| rs568653941 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9579787 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 146845 |
| rs568690356 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9631623 | GCTTAGTGGGTAGTT[C/G]GGCTAGGGGTGCAGG | 146845 |
| rs568894364 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641991 | GCAGCCAATGTGGCT[C/G]AGAAAGAAAAATCCA | 146845 |
| rs568920426 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9587258 | CCACATTTTCTTTAT[C/T]CAGTCTACCATTGAT | 146845 |
| rs568934906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586162 | TGATGATTTTATACC[C/T]GAGGTTGCAGCTTGT | 146845 |
| rs569008761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585544 | GGTGTGGTGGCGGGT[A/G]CCTGTAATCCCAGCT | 146845 |
| rs569015866 | snp | G/T | 1.70426e-05 | 0.00291908 | missense, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643030 | TTTTTCAGGTGGAAA[G/T]GACCATCTGGTCAAA | 146845 |
| rs569035081 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9613541 | GTTTGTTTTTGAAGC[A/G]GAGTCTTGCTCTGTC | 146845 |
| rs569096670 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9582361 | TTTGGTGGATATGAC[A/G]TGGTATCTCATTTCG | 146845 |
| rs569131953 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586513 | ATGTTGCAGTGAGCA[C/G]AGATCTCGCCATTGC | 146845 |
| rs569136981 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9605241 | CTGTGATACATCCAA[A/C]CAATGGCATATTAAT | 146845 |
| rs569254647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9629885 | GTGAGCCACTGCACC[C/T]GGTCCTCACTCCTCT | 146845 |
| rs569256602 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CFAP52 | GRCh38.p7 | 17:9635993 | GCCTGGCCAACATGG[C/T]GAAACCCCTTCTCTA | 146845 |
| rs569292086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9641086 | TTCACAAAGTTTAAG[A/G]TACAAAGGCAGTATA | 146845 |
| rs569345499 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9616022 | GAATAGGAACAGCTC[C/T]GGTCTACAGCTCCCA | 146845 |
| rs569349862 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9587938 | TCAAAGTTGGCTGCA[A/T]GTTGAAATCACCTGG | 146845 |
| rs569395621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9612794 | ACAGACAGTCCCTGA[C/T]TTATGATTTTTTTTA | 146845 |
| rs569400249 | snp | C/T | 1.65214e-05 | 0.0028741 | intron-variant | CFAP52 | GRCh38.p7 | 17:9612301 | TACTTTTGTGCTTCT[C/T]CCTAAAGGAAGATTC | 146845 |
| rs569407375 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642285 | CATGCCGATTGGAAC[A/G]TCATTATCATTTCCT | 146845 |
| rs569426203 | snp | G/T | | | missense | CFAP52 | GRCh38.p7 | 17:9632955 | GTATGTCATTAACAA[G/T]GCTCACAGGATCGGC | 146845 |
| rs569454129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9611664 | AACAACTGTACAAGC[C/T]CTGAAATGATTTTAC | 146845 |
| rs569459297 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9584735 | CCAGTGATTCTCCTG[C/T]CTCAGCCTCCCGAGT | 146845 |
| rs569539483 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9623756 | AGTGTCCATTCACCC[A/G]CATGATCATAGCACA | 146845 |
| rs569562043 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9574933 | TTGGAATCCATTCTT[C/G]TAATATCCAGGATGT | 146845 |
| rs569671466 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | CFAP52 | GRCh38.p7 | 17:9618166 | GAAGATCTACCAAGC[A/C]AATGGAAAACAAAAA | 146845 |
| rs569714875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9610711 | AGCTAATTTTTTTTT[A/G]TATTTTTAGTAGAGA | 146845 |
| rs569720540 | in-del | -/TACAGGCACGCTCCTGCCTCAGCCTCCCAAGTATCTGGGAC | 0.0352966 | 0.128072 | intron-variant | CFAP52 | GRCh38.p7 | 17:9629686 | CAGAGTAGCTGGGAT[lengthTooLong]TACAGGCGTGTGTCA | 146845 |
| rs569723597 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9597973 | TAGAGTGGGTAGTGT[G/T]CACTTCAGAGTGAGA | 146845 |
| rs569747486 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9640605 | GCTGCATAGTATTCC[A/G]TGGTATATATCTGCC | 146845 |
| rs569757932 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9579115 | GTGGGGATTGGGGAG[C/T]TTATGATTTTATTTT | 146845 |
| rs569777383 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9600618 | CGCCCAGGCTGGCGT[A/G]CAGTGGCGAGATGTC | 146845 |
| rs569822356 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9608858 | TGGTCTTTGTCCTCC[A/C]AGAACTTACAGACTC | 146845 |
| rs569837556 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9604515 | GCTTGTGCCTGTAAT[A/C]CCAGCACTTTGGGAG | 146845 |
| rs569909888 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633960 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGCGCC | 146845 |
| rs570007723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9595125 | CCAACTCCTGACCTC[A/G]GGTGCCTGTTTGGAG | 146845 |
| rs570032583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633552 | GAAAGGACGTTTACA[A/G]TACAGACATGAAAGT | 146845 |
| rs570044820 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9639954 | GTGGGTGTGAATCCT[A/G]AGAAACATGGGTTCT | 146845 |
| rs570056398 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9611974 | ATTTTTCAGAAGTGG[A/C]ATTAATAAAGGGGTT | 146845 |
| rs570145960 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CFAP52 | GRCh38.p7 | 17:9601915 | CACATAGCAGATATT[C/T]TCAAGAAACTTTGAA | 146845 |
| rs570211567 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9628278 | AGGCATCCTTCCCTA[A/T]ATTCTTTTTTTTTTT | 146845 |
| rs570225453 | snp | C/G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9640895 | GCAACGGGCCCAACT[C/G/T]GGCTTCCCAAAGTGC | 146845 |
| rs570234046 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9578702 | AAGCACCCACCACCA[A/C]GCCTGGCTAATTTTT | 146845 |
| rs570250941 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9589161 | AATGCAAGACATTCC[C/T]ATGTAAATGTCAAAG | 146845 |
| rs570316236 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9603797 | CTATGTAACAAACCC[G/T]CATGTTCTGCACATG | 146845 |
| rs570453479 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9610776 | ACTCCTGACCTCAGA[A/T]GATCCACCCACCTTG | 146845 |
| rs570542122 | snp | A/T | 1.66466e-05 | 0.00288496 | intron-variant | CFAP52 | GRCh38.p7 | 17:9635589 | GGAGGATGCAGTGAT[A/T]CCTGCAAAATCCAAT | 146845 |
| rs570600888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9595546 | TAAGCCAGGGTTTTA[C/T]AGGGTTCTTTCTGCT | 146845 |
| rs570615730 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9591252 | CATGTTGGTCAGGCT[G/T]GTCTCGAACTCCCAA | 146845 |
| rs570680782 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9641180 | CCAACAGGGAACCAA[C/G]GTTACCAGTTCCTCT | 146845 |
| rs570745396 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | CFAP52 | GRCh38.p7 | 17:9592158 | AGAATGTTTTCAACA[A/C]CCCAAAAAGAAACCC | 146845 |
| rs570750808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9622448 | CTAGTCCCAGCTACT[C/T]GGGAGGCTAAGGTGG | 146845 |
| rs570753117 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598519 | GTAATCCCAGCATTT[G/T]GGGAGGCGGAGGTGG | 146845 |
| rs570910207 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9614749 | TTAAAGGATGTTTGG[C/T]AGCATTCCTGGGCTC | 146845 |
| rs570925976 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9596051 | TGTATGTAGATATAT[A/G]TGTGTGTGTATATAT | 146845 |
| rs570976206 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9579764 | ATAGACACGGTGTTT[C/T]GCCACGTTGGCCAGG | 146845 |
| rs571009052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9634001 | TATCTTTTAAAGCAG[A/G]TGATGGTTTTAGCAT | 146845 |
| rs571033870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585458 | CGGATCACGAGGTCA[A/G]CAGTTCAAGACCAGC | 146845 |
| rs571080625 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP52 | GRCh38.p7 | 17:9579721 | TACAGGTATCCACCA[C/T]CACGCCTGGCTAATT | 146845 |
| rs571100405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9590336 | AGGCTTATGGATAAT[C/T]AGCCCATCTTTGATC | 146845 |
| rs571134781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9602571 | TTGCTATTGTGAATA[A/G]TGCCACAATAAACAT | 146845 |
| rs571161159 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585531 | AAAAAATTAGCCAGG[C/T]GTGGTGGCGGGTGCC | 146845 |
| rs571239857 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | CFAP52 | GRCh38.p7 | 17:9627217 | GAAAATTTTAATAAG[A/T]TTGTCTGCTTGGCTG | 146845 |
| rs571241718 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633326 | TCTCCTGCCTCAGCC[G/T]CCTGAGCAGCTGGGA | 146845 |
| rs571246196 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584746 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 146845 |
| rs571250297 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9640387 | CTTCCTGATGCTCTT[C/T]CTCCCCCCACCCACC | 146845 |
| rs571260547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9615339 | AATATTCATTACAGA[A/G]ACGTGCATTGCAGCA | 146845 |
| rs571305628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9628000 | TGGCCTCCCAAAGTG[C/T]TGGGATTACAGGTGT | 146845 |
| rs571405593 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9606307 | AGAATTGCTTCATCC[C/T]GGGAGTTCGTGGTTA | 146845 |
| rs571449705 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9609718 | TCTCAATTTTTTTTT[A/T]AAATAAAAAAGCAGT | 146845 |
| rs571581399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9607334 | CTGAGTGACAGAGAG[A/G]GACTCTGCCTCAAAA | 146845 |
| rs571766383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9593989 | ACAATAACAACAACA[A/G]CAAAAAACTTTTAAT | 146845 |
| rs571799409 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9584712 | CTGCAACCTCCGCCT[C/T]GTGGGTTCCAGTGAT | 146845 |
| rs571823958 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9588033 | CTCTAAGAGTTATAC[A/T]AGCTTCCCAGTACTG | 146845 |
| rs571852514 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585538 | TAGCCAGGTGTGGTG[A/G]CGGGTGCCTGTAATC | 146845 |
| rs571881314 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9595647 | AATACTTGAATTTTA[A/T]ATTAAAAAAAAAGTT | 146845 |
| rs571883622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9594843 | GAGGGAATAAATTAA[C/T]TTACAGATTCACTAA | 146845 |
| rs571906038 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9582046 | TTTCTGCTACATTTA[C/G]CCAGAGTTGACTCTT | 146845 |
| rs571959224 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9601205 | CTCATAGGTGGGAAT[G/T]GAACAATGAGAACAC | 146845 |
| rs572121420 | snp | A/G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9626192 | TAGGCTTGACTGCCA[A/G/T]GGAAGTGGATAGGCC | 146845 |
| rs572130881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9627275 | AGCACTTTGGGAGGC[C/T]GATGTGGGTGGATCA | 146845 |
| rs572165376 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9603310 | GCCTCCAGAGTTTAC[A/G]CCATTCTCCTGACTC | 146845 |
| rs572188339 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9589553 | GCCTAGCCAACATGG[C/T]GAGACCCCATCTCTA | 146845 |
| rs572274368 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9639453 | AAAAAAAATTCTACA[A/T]ATGGTACAGATTTCC | 146845 |
| rs572301055 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9592981 | ATGGTATCTGTTAAT[A/G]TCCCACTGTGGAAAA | 146845 |
| rs572306957 | in-del | -/A | 0.00199481 | 0.0315187 | upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576316 | ATCAATTATATATAT[-/A]TTTTTATAGCAGCCT | 146845 |
| rs572412822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638769 | GAAAAGCAGTGAGGC[A/G]TTGTGGTGGAGGGTG | 146845 |
| rs572442275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9593496 | AGTCTCGCTCTCTTG[C/T]CCAGGCTGGAGTGCA | 146845 |
| rs572457052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600875 | TTGGCCAGTTCTCTA[C/T]GCCCTCGTCTCTGGT | 146845 |
| rs572497338 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9598350 | TAAGTATTAATTTAA[A/G]TATTAAGTAACAATT | 146845 |
| rs572502333 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9594087 | GTTCGTTTTTAAGTA[A/T]CCTGTTGTGTTTTTT | 146845 |
| rs572506238 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9587641 | ATTGAGCCTTTTTTC[A/C]TATGCTTGTTGGCTG | 146845 |
| rs572559080 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9577777 | CACTTGTTGAGCCAA[A/T]GTAGAACCACACACA | 146845 |
| rs572592647 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9631534 | CAGGCAGAGGGAATA[C/G]CAAGTGCAAAGGCCC | 146845 |
| rs572603771 | in-del | -/AAAT | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9604755 | ACTCTGTCTCAAAAT[-/AAAT]AAATAAATAAATAAA | 146845 |
| rs572616338 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9637955 | CCCTCTTGGGGGCAC[C/G]CTGGGCAGGGTAGGG | 146845 |
| rs572658563 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9609190 | TTCACGGGGTACCAG[A/G]CATCATTCTAGGTGC | 146845 |
| rs572703622 | snp | A/G | 0.000965802 | 0.0219538 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586849 | GGTAATGAACTAAAC[A/G]TAGTTACTTATTTTC | 146845 |
| rs572767481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9581798 | CTAATTCCTTGGCAG[C/T]CAATTGAGAGATGTA | 146845 |
| rs572883315 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575570 | GATTTGGCGTAAGTC[C/T]TCAGCTCTCCAGCGG | 146845 |
| rs572892013 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9585682 | TGTCACACACACACA[C/T]ACACACAAAGTGTTG | 146845 |
| rs573001906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9606916 | TTTCTCTTCTCAATC[A/G]CAAAATGTCTTTTGA | 146845 |
| rs573035915 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9574628 | CAACCTACACCTCCC[A/G]GGTTCAAGCGATTCT | 146845 |
| rs573068529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9591473 | CCACACACGTAGATA[C/T]AGATCTCATTCTTTG | 146845 |
| rs573068546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9599557 | CGAATATTTCCTCCC[A/G]TTCTATGTGTAGCCC | 146845 |
| rs573171131 | snp | A/C | 0.000227195 | 0.0106558 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575824 | CCTGCAGACTCCGCC[A/C]GCCGCTCGGACTCTT | 146845 |
| rs573230027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9604945 | ACACTAACAACACCT[A/G]ATATTGACAGAGATG | 146845 |
| rs573235472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9580647 | TGAGCCATCACTGTA[C/T]CACTGCACTCCTGCC | 146845 |
| rs573269219 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9630274 | AGCCAGAAGCCAGAG[G/T]TCTGTTTTAAAATGT | 146845 |
| rs573398722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9581820 | AGAGATGTAACATAA[C/T]TGGCTCAGCCAATCA | 146845 |
| rs573483993 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9607705 | TATGCTTATACCTTC[C/T]CTTGGCTGCATTTGA | 146845 |
| rs573546672 | snp | C/T | 0.000112581 | 0.00750185 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575840 | GCCGCTCGGACTCTT[C/T]CTGCTCTTAGCAGCT | 146845 |
| rs573619354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641584 | ACCCCCTGCTGTAGC[C/T]TATTTATAATTTCAG | 146845 |
| rs573685513 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9631743 | TGGATTTTAATTCTA[A/C]GTGCAGTGGGAAAAT | 146845 |
| rs573698440 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9625167 | ATTGACCCCATGTAG[A/C]TGTCTTTAGCAGTAG | 146845 |
| rs573764169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600882 | GTTCTCTATGCCCTC[A/G]TCTCTGGTTTTTATT | 146845 |
| rs573788480 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B | CFAP52, USP43 | GRCh38.p7 | 17:9643405 | ATTTGTGCAGACTCT[A/C]ATTAGAACTTTTAAC | 146845 |
| rs573827488 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | CFAP52 | GRCh38.p7 | 17:9593716 | CCGCCTCGGCCTCCC[A/C]AAGTGCTGGGATTAC | 146845 |
| rs573839749 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9598934 | AGCCCGTGGCACTCA[G/T]AGCCCACAGCACATT | 146845 |
| rs574027661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9599706 | ACAGGTGTTCATGGG[C/T]ATCATTCAGGGCATC | 146845 |
| rs574033194 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9640966 | TCGCATTTTCTTTAT[A/G]CAGTCTATCATTGAT | 146845 |
| rs574065055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9605440 | GATCAGGCTGGGCGC[A/G]GTGGCTGACACCACT | 146845 |
| rs574100353 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CFAP52 | GRCh38.p7 | 17:9635281 | CCCACCCAACCGAGA[C/T]AAAGACAGGGAATTA | 146845 |
| rs574142021 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9611867 | ATTCCATTACAACTG[A/G]GTATTTAGGTTGTTT | 146845 |
| rs574197614 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9603958 | TGGTGAAAGAATAGA[C/T]AAATGGATCAATGGG | 146845 |
| rs574234830 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9640819 | CAGCTAATTTTTGTA[A/T]TTTTAGTACAGACAG | 146845 |
| rs574244314 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9578291 | GTCAAAAGGCCTTTT[C/G]AGGACATGACGGCAC | 146845 |
| rs574264673 | snp | A/G | 1.64768e-05 | 0.00287021 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600200 | TGAGTAGAGACCATC[A/G]CCACTGCCCTGCCAT | 146845 |
| rs574278593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9636813 | GCACTTTGGGAGGCC[A/G]AGGTGGGAGGATCAA | 146845 |
| rs574356474 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642107 | TATTTTTGGTGGGCA[C/T]TGATAATAGAAATGG | 146845 |
| rs574357932 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CFAP52 | GRCh38.p7 | 17:9635723 | GGTCCATGGTTTATC[C/G]ATGCTAGTGGGGAGG | 146845 |
| rs574418150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9636488 | TTGTAGGAGTAACTC[A/G]AAGGATTTTTGAACA | 146845 |
| rs574447947 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585472 | AGCAGTTCAAGACCA[G/T]CCTGACCAACATGGT | 146845 |
| rs574455166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9590773 | AAATTTGTTTGCAGA[A/G]CATTCAAGAATGTTG | 146845 |
| rs574514805 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CFAP52 | GRCh38.p7 | 17:9626938 | GTAGACATTGCTTGA[A/G]ATGTACTGAAATCTA | 146845 |
| rs574517538 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CFAP52 | GRCh38.p7 | 17:9591289 | GTGATCCACCCTCCT[C/T]GGCCTCCCAAAGTGC | 146845 |
| rs574519687 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585671 | GTGCAAGACTCTGTC[A/T]CACACACACACACAC | 146845 |
| rs574566185 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9614501 | ACTTAGTCTGATATT[A/G]AGATTACCACATCTT | 146845 |
| rs574614738 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | CFAP52 | GRCh38.p7 | 17:9629714 | CTGCCTCAGCCTCCC[A/G]AGTATCTGGGACTAC | 146845 |
| rs574642594 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9589049 | AGAGGTTGCAGTGAG[C/T]GAAGATTGCACCACT | 146845 |
| rs574662311 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9626585 | TTTCATGAGTGGTCC[A/G]TGAGTACACCTCTTT | 146845 |
| rs574708905 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9630031 | CTCAGGACAGAAATC[C/T]TGGAGTCCTCACTGC | 146845 |
| rs574709931 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9578850 | CACACCCAGCCACAG[C/G]GTGGAGGGGTGCATG | 146845 |
| rs574750057 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9621966 | ATATGTAACTAACCT[G/T]CACAATGTGCACATG | 146845 |
| rs574780604 | snp | C/T | 0.000648363 | 0.0179934 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586000 | AAAACGACTCATTGT[C/T]AATTTATCTAGAGGT | 146845 |
| rs574831256 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585225 | TCTCAACCCCTTCTC[A/C]GACCTGAAATCAGAA | 146845 |
| rs574869940 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9628427 | TGGGATTACAGGCAT[C/G]CACCACCATACCCGG | 146845 |
| rs574890793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9636331 | AATGAACTTCCCATG[A/G]AGGGGAGGGATGCTG | 146845 |
| rs574905572 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9634152 | TCTCCTCCTCTGTGC[A/C]CCAGATTCTTTGCTA | 146845 |
| rs574922743 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9603511 | ACCACACCCGGCCCT[A/C]AGTAGATATTTCATG | 146845 |
| rs574982332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9597586 | GAAGCGGATGGATCA[C/T]GAGGTCAAGAGATGG | 146845 |
| rs575027103 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9603954 | GGGTTGGTGAAAGAA[C/T]AGATAAATGGATCAA | 146845 |
| rs575031645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9635785 | AAGTTTCTGGGCAGA[C/T]AGGGAAATAGCTTTC | 146845 |
| rs575066970 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642609 | AGCCTGAGTGACAGA[C/T]AGTCCGTCTCAATAA | 146845 |
| rs575106576 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9578236 | ATTCACCTTGGGATG[A/G]AGACCTAACATTTAA | 146845 |
| rs575128166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586065 | TAGTTCTATGTGGCA[A/G]TGTGCTTTATTCTTC | 146845 |
| rs575198837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9579810 | TGACCTCAGGTGATC[C/T]ACCCGCCTCGGCCTC | 146845 |
| rs575214572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9610467 | ATGAGAAGTCATGGA[A/G]ACTGGAAAGGGAAGA | 146845 |
| rs575271132 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9641478 | ATCAAAAGCCCTTTC[G/T]GTCTTAATCCAGGTT | 146845 |
| rs575283323 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP52 | GRCh38.p7 | 17:9608882 | CAGACTCGTTTGGGG[C/T]TAAGGTATGTACACA | 146845 |
| rs575309991 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9579375 | GCCTGGTTGCAGAAC[A/G]GCAAATAGCTTGGGG | 146845 |
| rs575324329 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9624948 | GTCAACCAAGGGTTT[A/G/T]TGCAGAGATGAAGCT | 146845 |
| rs575400696 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | CFAP52 | GRCh38.p7 | 17:9604811 | AATAAATAAAAGAAG[A/T]TATACAGATGGCAAG | 146845 |
| rs575537698 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9604154 | TCACAAAAATTAACT[A/C]AAAATGGATTACAGA | 146845 |
| rs575553152 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9605506 | ATCATGAGGTCAAGA[A/G]ATCAAGACCATCCTG | 146845 |
| rs575603311 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP52 | GRCh38.p7 | 17:9593478 | TTTTTGTTTTCGAGA[C/T]GCAGTCTCGCTCTCT | 146845 |
| rs575667870 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9622082 | TAATCTGCCAAAAAG[G/T]CAAGAGTCTCAGCAT | 146845 |
| rs575672256 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9585385 | CTTATTTTTAAAGTG[G/T]TGGCCGGGCGCGGTG | 146845 |
| rs575681387 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9626325 | ACCTCCGCCTCCTGG[A/G]TTCAAGTGATTCTCC | 146845 |
| rs575759823 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9640876 | CTCGCATTCCTGACC[A/T]CAAGCAACGGGCCCA | 146845 |
| rs575776565 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9591016 | ATAGTGGACATCCTA[G/T]AGTTTGCATGCATCT | 146845 |
| rs575825704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9629646 | TCTGCCTCCCGTGTT[C/T]AAGCAATTCTCCTGT | 146845 |
| rs575870684 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585487 | GCCTGACCAACATGG[C/T]GAAACCCCGTCTCTA | 146845 |
| rs576013139 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9613366 | TTTGTCTTTGGTGAG[A/G]TTCATTTCATGAAGT | 146845 |
| rs576020054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632471 | TCCCTGCATAAATAA[A/G]TGGTTGTAAGCAAGA | 146845 |
| rs576022292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638523 | CCAACCCAAATCCCA[A/G]CTTGCACCAAATCCA | 146845 |
| rs576072731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9602833 | TGAGATGGTATCGCA[C/T]TGCAGTTTTGATTTA | 146845 |
| rs576159783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9590008 | TCTTGGATCTGTGGG[C/T]CTGAGCCTGTTCAGC | 146845 |
| rs576162288 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638022 | CAAGGGTTGAGCCTG[C/T]CAGCTTTTGGGACAT | 146845 |
| rs576209110 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9609244 | CATAAAAGATGAAAA[A/C]AAAAATCCCTGTCCT | 146845 |
| rs576284692 | snp | A/G | 0.00013202 | 0.00812357 | missense | CFAP52 | GRCh38.p7 | 17:9632983 | GGCGTCACCGCCATC[A/G]CCACCACCAGTGACT | 146845 |
| rs576296168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9597164 | AGTCATGCAGTGTTT[A/G]TTTTTCTGTGCTTGC | 146845 |
| rs576432580 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633823 | CTGGGACTACAGGTG[C/T]CTGCCACCACGCCCA | 146845 |
| rs576470234 | snp | A/G | 1.64795e-05 | 0.00287045 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9594244 | CTGTGGCAGCCCTGC[A/G]GCCGGCCTCAATGTT | 146845 |
| rs576497750 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9622186 | AGTCTCTCTCTCTCT[C/T]TTTAACACATCAATC | 146845 |
| rs576609317 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9601473 | AAAGCATAGGGCCTA[C/T]TGCTTTGTGATTTTA | 146845 |
| rs576618996 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | CFAP52 | GRCh38.p7 | 17:9616023 | AATAGGAACAGCTCC[G/T]GTCTACAGCTCCCAG | 146845 |
| rs576622649 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9613627 | GATTCAAGCGATTCT[C/T]CTGCCTCAGCCTCCT | 146845 |
| rs576636312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9579830 | GCCTCGGCCTCCCAA[A/G]GTGCTGGGATTACAG | 146845 |
| rs576650394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9577890 | TGAGGTCAGGAGTTC[A/G]AGACCATCCTGTCCA | 146845 |
| rs576697149 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575844 | CTCGGACTCTTCCTG[C/T]TCTTAGCAGCTGACT | 146845 |
| rs576806771 | snp | A/C | 0.00356998 | 0.042098 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584396 | CAGAACTGAAACCGA[A/C]AGTTAAAAAAATTAT | 146845 |
| rs576814894 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633649 | TTTTCCTCCGAGGAT[C/T]GTGGTTGTACGAATT | 146845 |
| rs576876814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9597417 | GAGATAATGCATATG[C/T]TCAATAGCTTGATTT | 146845 |
| rs576922160 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9585434 | AGCACTTTGGGAGGC[C/T]AAGGTGGACGGATCA | 146845 |
| rs576949574 | snp | A/G/T | 3.4571e-05 | 0.00415744 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633064 | ATTTGAAAAAATAAC[A/G/T]CTCTGTTTAGAACAA | 146845 |
| rs576991438 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9594567 | AACTGTTCTCAGGTT[C/G]TTGTTTGTGACAGAA | 146845 |
| rs577000912 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9621903 | AGATATACCTAATGC[G/T]AGATGACACGTTAGT | 146845 |
| rs577054095 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585496 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 146845 |
| rs577055515 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9622171 | ATCTTTGCTATTATC[A/G]GTCTCTCTCTCTCTT | 146845 |
| rs577116370 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584561 | TAGTTACTTTTTGTG[G/T]GTGATGAAAACACTT | 146845 |
| rs577121006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9589294 | TTATTACAAAGGAAA[C/T]TTATATTTGTGTATA | 146845 |
| rs577184423 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585031 | AAAATAGGCCAAATT[C/T]TTATATTTACCCAAC | 146845 |
| rs577201488 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9590729 | ATCTGGCAAAACTGT[G/T]AATCTCTGCTGTAAT | 146845 |
| rs577255787 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9588672 | TTCAATTTCACCCCA[G/T]TCAGTGTGATAATTT | 146845 |
| rs577320436 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9578448 | GCTTCAGTTAGTAAG[G/T]GCCTATGAACTGGAC | 146845 |
| rs577343571 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9609405 | TATGGTTTGAATAGA[A/G]GCAGGGAGGCCAGGT | 146845 |
| rs577385262 | snp | C/T | 8.28411e-05 | 0.00643535 | intron-variant | CFAP52 | GRCh38.p7 | 17:9594333 | GAAAGTATGTGTCTG[C/T]GTTCGGAGTTTTCAG | 146845 |
| rs577483451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9616148 | TGTGTGCGCGCACCG[C/T]GCGCGAGCCGAAGCA | 146845 |
| rs577555141 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9603002 | TTAAGGAGAGCAAGT[C/G]TTAGAGCCCTGCCAG | 146845 |
| rs577609529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9578745 | GAGACGGGGTTTCAC[C/T]AAGTTGGCCAGACTA | 146845 |
| rs577680393 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9614138 | TTTCCTTTTCCTTTT[C/G]TTTTTCTTTTCTTTC | 146845 |
| rs577682066 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CFAP52 | GRCh38.p7 | 17:9636772 | CAAAGCACTGCTGGG[C/T]GCGGTGGCTCCCGCC | 146845 |
| rs577765592 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632299 | TGGGTCTTGCCATGT[C/T]TCCAGGCTGGTCTTG | 146845 |
| rs577830203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9582740 | CTCCCAGGTTTAAGC[A/G]ATTCTCCTGCCTCAG | 146845 |
| rs577982109 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9599437 | GGGGCACACCTTTAT[C/T]CTAGGAGCCCTTAAG | 146845 |
| rs578043543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600243 | ACTGGCAGCATGTAC[C/T]TTTTTTTTTCCTTTT | 146845 |
| rs578043870 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9608626 | GCAAAGCATTGTGTT[A/G]ATCATGCATTTGAAT | 146845 |
| rs578129700 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9581441 | AAGATGTCAAAGATA[C/T]ATTAAGTATAAAATG | 146845 |
| rs578144774 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9599905 | CACCACGACACCCAG[A/C]TAATTTTGTATTTTC | 146845 |
| rs578178723 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9593479 | TTTTGTTTTCGAGAC[A/G]CAGTCTCGCTCTCTT | 146845 |
| rs578209806 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9631967 | TAGTAGAGGTGGGGT[C/T]TTGCCATGTTGACCA | 146845 |
| rs578214036 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9637227 | AGTGCTGGTTCAAGG[A/T]CCACACTTGTAGGAA | 146845 |
| rs578256566 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9631395 | CTCACCCCCTCACCT[C/T]CTCAAATCTTTGCTG | 146845 |
| rs745330016 | snp | C/T | 0.000148306 | 0.00860993 | missense, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641800 | GGTCGATAAATGGCA[C/T]GGATATCACACAGGA | 146845 |
| rs745480697 | in-del | -/TCAGATGGAGTT | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9629564 | TTTTTTTTTTTTTTC[-/TCAGATGGAGTT]TCACTCTTGTTGCCC | 146845 |
| rs745505537 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9581380 | GCAATTTGATACTGT[A/G]CAATCCTTAAGAAAA | 146845 |
| rs745505604 | snp | A/G | 3.29544e-05 | 0.00405908 | missense | CFAP52 | GRCh38.p7 | 17:9594260 | GCCGGCCTCAATGTT[A/G]GCAATGCCACCAATG | 146845 |
| rs745561888 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9635288 | AACCGAGACAAAGAC[A/C]GGGAATTAAAAAAAC | 146845 |
| rs745586152 | snp | A/C | 5.08083e-05 | 0.00504 | utr-variant-5-prime, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576673 | ACTAGGGAGGAGAGC[A/C]AAGTAATCAGAACCT | 146845 |
| rs745596409 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9598544 | AGGTGGGTGAATCAC[C/T]TGAGGTCATGAGTTC | 146845 |
| rs745601919 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9627865 | AGCCAGGACCACAGG[C/T]ATGCATCACTACACC | 146845 |
| rs745651699 | snp | A/C | | | downstream-variant-500B, upstream-variant-2KB, intron-variant | CFAP52, USP43 | GRCh38.p7 | 17:9643589 | TTCATTGGTCAAGCT[A/C]TATGGGACTAGACTC | 146845 |
| rs745689614 | snp | C/T | 1.64749e-05 | 0.00287005 | intron-variant, missense | CFAP52 | GRCh38.p7 | 17:9585878 | CTAAAGAGCAGAACT[C/T]CCTACAGGGTCATGG | 146845 |
| rs745698329 | in-del | -/GA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9609992 | AATCTGATTTCTGGA[-/GA]GAGAGAGAGAGAGAG | 146845 |
| rs745722527 | in-del | -/G | 3.31559e-05 | 0.00407147 | intron-variant | CFAP52 | GRCh38.p7 | 17:9612491 | ATTGTGAGTAGAAGA[-/G]GAAAAACAAGAATGT | 146845 |
| rs745738813 | snp | A/G | | | intron-variant, missense | CFAP52 | GRCh38.p7 | 17:9585929 | CCATCTCCAGGTCTG[A/G]AGAGTACATCGCCTC | 146845 |
| rs745745841 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9633163 | AATTGACATTTTGAT[A/G]AGATCTGAAAATATG | 146845 |
| rs745747701 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9626949 | TTGAGATGTACTGAA[A/T]TCTAAAAATTAGCTT | 146845 |
| rs745771020 | snp | C/T | | | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575381 | CCTCGGTTTCTCCAC[C/T]TGTGAAATAAGGGGG | 146845 |
| rs745777390 | in-del | -/TT | 0.000823254 | 0.0202719 | intron-variant | CFAP52 | GRCh38.p7 | 17:9594162 | TGTTTTCTCTTTGAC[-/TT]TTTTTTTTTGGTCCC | 146845 |
| rs745787264 | snp | A/G | 1.68139e-05 | 0.00289943 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641704 | TGAGTCCTGCTTAAT[A/G]CTTCTTTCCTGAATT | 146845 |
| rs745825279 | in-del | -/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9587205 | CTCATGATCTCATTC[-/T]TTTTTATGGCTGCGT | 146845 |
| rs745837621 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9606619 | GATTTCAACCCAGGC[C/T]GACTGGCTGCAGAAC | 146845 |
| rs745840181 | snp | A/G | 1.64727e-05 | 0.00286986 | splice-donor-variant | CFAP52 | GRCh38.p7 | 17:9612480 | TATTGTCTTTCCATT[A/G]TGAGTAGAAGAGAAA | 146845 |
| rs745862730 | snp | A/G | | | upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576288 | CACTGCTCCAAACAG[A/G]GGCCCAAAGAAGTAT | 146845 |
| rs745892532 | snp | C/G | | | intron-variant, synonymous-codon | CFAP52 | GRCh38.p7 | 17:9585792 | TGTGCCCACTGGTCT[C/G]AAATGCCATCCTGAC | 146845 |
| rs746005999 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9638518 | ATAAACCAACCCAAA[C/T]CCCAGCTTGCACCAA | 146845 |
| rs746074979 | snp | A/T | 3.3012e-05 | 0.00406262 | intron-variant | CFAP52 | GRCh38.p7 | 17:9628832 | TCAGGTAACGTCCAC[A/T]TGTCAAGATCTGGCT | 146845 |
| rs746078846 | snp | A/C | 3.29614e-05 | 0.00405951 | synonymous-codon, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643114 | CAACATCACACGCAT[A/C]CGCATAAGTCCAGGA | 146845 |
| rs746126670 | snp | A/G | 1.65828e-05 | 0.00287943 | splice-acceptor-variant | CFAP52 | GRCh38.p7 | 17:9632886 | TTTCCCTTTCATGCC[A/G]GCATGGAACGACGGT | 146845 |
| rs746183243 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9603514 | ACACCCGGCCCTAAG[C/T]AGATATTTCATGTTC | 146845 |
| rs746199123 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9579715 | TGGGATTACAGGTAT[C/T]CACCACCACGCCTGG | 146845 |
| rs746203400 | snp | A/G | 1.64906e-05 | 0.00287142 | intron-variant | CFAP52 | GRCh38.p7 | 17:9635381 | CCAAGTGTGGATCAA[A/G]ATCCTGTGCTCTGTG | 146845 |
| rs746253693 | snp | C/T | 1.66563e-05 | 0.0028858 | missense, upstream-variant-2KB, utr-variant-5-prime | CFAP52, STX8 | GRCh38.p7 | 17:9576736 | CCCAAGTGGCGGAGC[C/T]GGAACTTGACGCCGT | 146845 |
| rs746315199 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9582537 | TTGTAGGAGTTCTTC[A/G]TATATTATGGAGATG | 146845 |
| rs746362333 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9589876 | ATCACCAAGAGTGCT[A/G]TCTACAGACAAGAAA | 146845 |
| rs746370813 | snp | A/G | 1.65162e-05 | 0.00287365 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9608163 | GGGGGGTTTGTTGGT[A/G]GGCTCTGGAGCCGGA | 146845 |
| rs746423900 | snp | C/T | 1.70682e-05 | 0.00292127 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586660 | CTCAGATGCTTTTAA[C/T]GCCTCCCTATGATCT | 146845 |
| rs746428435 | snp | A/C | 0.000140934 | 0.00839329 | intron-variant | CFAP52 | GRCh38.p7 | 17:9608257 | TGGGGCTGGGTAGAG[A/C]CCCACTAAACGGAGA | 146845 |
| rs746523607 | snp | A/G | 3.33884e-05 | 0.00408572 | utr-variant-5-prime, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576695 | TCAGAACCTCCCAAG[A/G]ATGGATAACAAAATT | 146845 |
| rs746542649 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9598215 | TGATTGTGGTTTTTT[G/T]TTTTTTTTTTTTACA | 146845 |
| rs746544544 | in-del | -/AAAGAA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631055 | GAGAGAGAGAGAGAG[-/AAAGAA]AGAAAGAAAGAAAGA | 146845 |
| rs746587861 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9613042 | ATGTTCAGTAGGTGA[A/G]GTGTATTAAGTGCAT | 146845 |
| rs746599103 | in-del | -/CA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636174 | AGTGAAACTCTGTCT[-/CA]AAAAAAAGAAAGAAA | 146845 |
| rs746608233 | snp | A/T | 1.67075e-05 | 0.00289023 | missense, upstream-variant-2KB, utr-variant-5-prime | CFAP52, STX8 | GRCh38.p7 | 17:9576751 | TGGAACTTGACGCCG[A/T]GATCGGCTTCAATGG | 146845 |
| rs746643469 | snp | C/T | 0.00016475 | 0.00907457 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9635503 | GGTGAAGAGGAACAA[C/T]GAGGAGTGTGTCACC | 146845 |
| rs746680204 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9593402 | CTGAATCAGAAACTG[C/T]GGTGCTGTGGCCTAG | 146845 |
| rs746705703 | in-del | -/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9607454 | TCATACATTGTCAAG[-/C]CCTTTTTTTTCTTTG | 146845 |
| rs746731802 | snp | A/G | 1.65677e-05 | 0.00287812 | splice-acceptor-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641722 | TCTTTCCTGAATTCC[A/G]GATTGCTTACTGGGA | 146845 |
| rs746761194 | snp | C/G | | | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575284 | CAATTTCCCTCCCAG[C/G]TTCCTGTATCTGGAA | 146845 |
| rs746932861 | snp | C/T | 1.64887e-05 | 0.00287125 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9628738 | GCACACATCATCCAA[C/T]AGGGAGCTGCTGCGG | 146845 |
| rs746958003 | in-del | -/GATCCACCCCCCTGGCCTCCCAAAGTGCTGGGATTACAGGTTTGAGCCA | 1.64996e-05 | 0.0028722 | intron-variant | CFAP52 | GRCh38.p7 | 17:9628827 | CATTTCAGGTAACGT[lengthTooLong]CCACATGTCAAGATC | 146845 |
| rs746970124 | in-del | -/AA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631050 | GAGAGAGAGAGAGAG[-/AA]AGAGAAAGAAAGAAA | 146845 |
| rs746987839 | snp | G/T | 8.25962e-05 | 0.00642583 | splice-donor-variant | CFAP52 | GRCh38.p7 | 17:9594322 | TATGACTGCTGGAAA[G/T]TATGTGTCTGCGTTC | 146845 |
| rs746987913 | snp | A/T | 1.64808e-05 | 0.00287057 | missense | CFAP52 | GRCh38.p7 | 17:9628790 | TGCCACGGCATCGAC[A/T]TCATGAGGGACGGCA | 146845 |
| rs747001263 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9625824 | TTTGTGAGAAAATGT[C/G]TGTGAACCAGTTCAG | 146845 |
| rs747062472 | snp | C/G | 1.64819e-05 | 0.00287066 | missense, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643128 | TCCGCATAAGTCCAG[C/G]AAATCAATATATTGT | 146845 |
| rs747062992 | snp | C/T | 5.04774e-05 | 0.00502356 | missense, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643187 | CGATGGAAGTACCCA[C/T]ATACCTCCTGAAGCT | 146845 |
| rs747187180 | snp | A/G | 1.64917e-05 | 0.00287151 | missense | CFAP52 | GRCh38.p7 | 17:9632968 | AATGCTCACAGGATC[A/G]GCGTCACCGCCATCG | 146845 |
| rs747220586 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9610926 | TTGTTGTCATCTGTG[A/G]GCTAGCAACAGATAT | 146845 |
| rs747224320 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9578288 | TATGTCAAAAGGCCT[C/T]TTCAGGACATGACGG | 146845 |
| rs747272721 | snp | A/C | 1.64746e-05 | 0.00287002 | stop-gained | CFAP52 | GRCh38.p7 | 17:9600093 | TGATAGCTTTTTCTA[A/C]CTTGGCACCACGACT | 146845 |
| rs747288047 | snp | A/C | | | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9577389 | GGGACTGGGCCGCTC[A/C]GCTGAAATCTTATTT | 146845 |
| rs747349187 | snp | A/G | 1.65515e-05 | 0.00287671 | intron-variant | CFAP52 | GRCh38.p7 | 17:9612295 | CTACTTTACTTTTGT[A/G]CTTCTCCCTAAAGGA | 146845 |
| rs747463227 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9640318 | GTGCCGTGGTGGTTT[A/G]CTGTACGGATCATCC | 146845 |
| rs747471710 | snp | A/T | 1.65045e-05 | 0.00287263 | missense | CFAP52 | GRCh38.p7 | 17:9586795 | CCTTTTCTCCAAATG[A/T]TTTGTACTTGGTATC | 146845 |
| rs747484892 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9603375 | CACCATGCCCAGCTA[A/C]CTTTTTTGTATTTTT | 146845 |
| rs747511528 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9602175 | ATACATGTGCAGACC[A/G]TGCAGGTTTGTTACA | 146845 |
| rs747632055 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642513 | CCTATAATCCCAGCT[A/G]CTTGGGAGGCTGAGA | 146845 |
| rs747690759 | snp | A/G | 1.65798e-05 | 0.00287917 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585725 | AAGTAGAAAATTCCT[A/G]GCCACTTCTGCACCT | 146845 |
| rs747738212 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9591791 | GCTGAAGTGGGAGGA[C/T]TGCTTGAGCCCAGGA | 146845 |
| rs747750432 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631684 | GCGGGGGTTGGGGGT[C/T]GGGCACAAATACTAG | 146845 |
| rs747782160 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9590073 | TCATGGATATGTTCC[A/G]TGAGAATCCAGTTGT | 146845 |
| rs747787922 | snp | A/C | 1.64963e-05 | 0.00287192 | missense | CFAP52 | GRCh38.p7 | 17:9612310 | GCTTCTCCCTAAAGG[A/C]AGATTCAGTTACAAG | 146845 |
| rs747834863 | snp | C/T | 1.64768e-05 | 0.00287021 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9612393 | AACAGAAGAATCGCA[C/T]ATTTATCGTGTCAGC | 146845 |
| rs747966332 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9624441 | CATCTCCAATCTGTC[A/G]TTGAGTCCACCTAGT | 146845 |
| rs747984041 | snp | C/G | 1.64863e-05 | 0.00287104 | missense | CFAP52 | GRCh38.p7 | 17:9628809 | TGAGGGACGGCAAAA[C/G]CATCATTTCAGGTAA | 146845 |
| rs748021031 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9635628 | CAGTTTATTGAACAT[C/G]AGAGAAGATTCACAT | 146845 |
| rs748029722 | snp | C/G | 1.68875e-05 | 0.00290576 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632861 | ATATACTGATCCTGC[C/G]TGCCTTTTGTTTCCC | 146845 |
| rs748081227 | snp | A/G | 1.67267e-05 | 0.0028919 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9598309 | CCAAACAGGACAGTT[A/G]AAAAGAATAGTCATG | 146845 |
| rs748096772 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9596467 | TGAAGTCTTTGTGAT[A/G]TTGGCCTTGAAATTT | 146845 |
| rs748194407 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9607220 | GCATGATGGCGCATG[C/T]CTATAATCCCAGCTA | 146845 |
| rs748195329 | snp | A/G | 1.76577e-05 | 0.00297129 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633079 | GCTCTGTTTAGAACA[A/G]CTGCCCTATAGGAAG | 146845 |
| rs748276400 | snp | C/T | 4.94181e-05 | 0.00497057 | missense | CFAP52 | GRCh38.p7 | 17:9600104 | TCTACCTTGGCACCA[C/T]GACTGGAGATATTCT | 146845 |
| rs748290034 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9594411 | GATCTGGGGGAACAC[A/G]TCTTTAGTCCTGGAT | 146845 |
| rs748312304 | in-del | -/TTTG | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9600557 | AAAGCACACACTTTG[-/TTTG]TTTGTTTGTTTGTTT | 146845 |
| rs748343871 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9628617 | TTTTGGTGTCAAATA[C/T]GCATCTGGGAAACTG | 146845 |
| rs748532407 | snp | A/C/G | 6.86146e-05 | 0.0058569 | intron-variant | CFAP52 | GRCh38.p7 | 17:9594145 | TTCTTATTTTAAAAG[A/C/G]CTGTTTTCTCTTTGA | 146845 |
| rs748540856 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9613982 | GTCTCACTTTTTCCC[C/T]TCTTTTTTTTTAATA | 146845 |
| rs748554545 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9586489 | GAAGTGCTTGAACCC[A/G]GGAGGTGGATGTTGC | 146845 |
| rs748587285 | snp | A/G | 1.64885e-05 | 0.00287123 | missense | CFAP52 | GRCh38.p7 | 17:9594224 | ATAGCCAAGAGAGAT[A/G]CCATCTGTGGCAGCC | 146845 |
| rs748625663 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9599601 | CTCAGAGCTGTTCTG[A/T]CCCATCTTTGAGCCT | 146845 |
| rs748704412 | snp | A/C | 3.29685e-05 | 0.00405995 | missense | CFAP52 | GRCh38.p7 | 17:9638677 | GCTATCACCCTGAGG[A/C]GTTCCAGATCATCAC | 146845 |
| rs748744567 | snp | A/C | 0.000110114 | 0.00741922 | upstream-variant-2KB, splice-donor-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575791 | CTCACCCGGGACTCA[A/C]CAGGGGTCCGGTGCC | 146845 |
| rs748750084 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9600721 | AGGCGCCCGCCACCA[C/T]GCCCAGCTAATTTTT | 146845 |
| rs748843341 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9578581 | TTATTTTGAGACGGT[A/G]GAGTCTCGCTCTGTT | 146845 |
| rs748844112 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9588374 | TCAGCCCGCTCGTGC[C/G]CAGAGAGACAAAGAG | 146845 |
| rs748884130 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9584155 | CAGAGTTGTTGGTCA[C/T]TGTATTTTCTTTTAT | 146845 |
| rs748934853 | snp | C/T | 5.11043e-05 | 0.00505465 | intron-variant | CFAP52 | GRCh38.p7 | 17:9594158 | AGCCTGTTTTCTCTT[C/T]GACTTTTTTTTTTTG | 146845 |
| rs748964845 | snp | C/T | 1.6483e-05 | 0.00287076 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9612459 | TCACTTTGATGCTGT[C/T]GAGGATATTGTCTTT | 146845 |
| rs748988202 | snp | C/T | 1.64808e-05 | 0.00287057 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9594241 | CATCTGTGGCAGCCC[C/T]GCAGCCGGCCTCAAT | 146845 |
| rs748991785 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9623539 | TTCAAGAAATTAAGA[C/G]AAGAAAAAATTTAAA | 146845 |
| rs749112015 | snp | G/T | 1.6489e-05 | 0.00287128 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9600069 | CTTGCTTCTTCAGGT[G/T]GATGATGATGATAGC | 146845 |
| rs749129732 | snp | A/G | 1.6736e-05 | 0.0028927 | missense | CFAP52 | GRCh38.p7 | 17:9598322 | TTGAAAAGAATAGTC[A/G]TGAGTATTGGAGTAA | 146845 |
| rs749174417 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9593627 | CATCCAGCTAATTTT[C/T]TTATTTTCAGTAAAG | 146845 |
| rs749180219 | snp | G/T | 1.65597e-05 | 0.00287743 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585734 | ATTCCTGGCCACTTC[G/T]GCACCTGATTATTAT | 146845 |
| rs749259768 | snp | C/T | 1.64879e-05 | 0.00287118 | missense | CFAP52 | GRCh38.p7 | 17:9594303 | GGTGCCGGGATGAGA[C/T]GTTTATGACTGCTGG | 146845 |
| rs749274721 | snp | C/T | | | upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576314 | AGTATCAATTATATA[C/T]ATTTTTTATAGCAGC | 146845 |
| rs749368606 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9639777 | GCAGCATCTGAGTGA[C/G]GCCTGAATGACAGAA | 146845 |
| rs749398701 | snp | G/T | 1.65209e-05 | 0.00287405 | missense | CFAP52 | GRCh38.p7 | 17:9608152 | TGCCTGAAGATGGGG[G/T]GTTTGTTGGTGGGCT | 146845 |
| rs749427640 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9628478 | AGAAACGGGGTTTCA[A/C]CATGTTGGTCAGGCT | 146845 |
| rs749471334 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9638723 | AAAGGTGAGTCCTCC[C/T]AGTGAGAGATGAGAT | 146845 |
| rs749510038 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9600597 | TGAGAAAGAGTCTCG[C/T]TCTGTCGCCCAGGCT | 146845 |
| rs749526553 | snp | C/G | | | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575496 | TAGCTCCAAAACCAG[C/G]ATGGGCGGGAAATCC | 146845 |
| rs749539026 | in-del | -/T | 0.000218429 | 0.0104483 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586869 | TACTTATTTTCTTTA[-/T]TTTTTTTAACTTTTA | 146845 |
| rs749551982 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9627187 | GAATTCTGGCACCAT[A/T]GTCTTTTCCTTTTTG | 146845 |
| rs749564994 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642480 | AACACAAAAATTAGC[C/T]GGGCGTGGTGGTGCA | 146845 |
| rs749647842 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9582882 | CCTCGAGTGATCTGC[C/G]TGCCTCGGCCTCCCA | 146845 |
| rs749684645 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9638046 | GGGACATCCCCACGT[G/T]ACAGGCTCGTGCTTT | 146845 |
| rs749690791 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9632816 | CCTGCCTCTCCTTAG[C/T]GAGGCCAGCAGACTG | 146845 |
| rs749691517 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9599290 | AGATTTTAGATTTTT[A/T]GATTTTTGGATTATA | 146845 |
| rs749800986 | in-del | -/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9579597 | TTTTGAGATGGAGTC[-/T]CACCCTGTCTCCCAG | 146845 |
| rs749849724 | snp | A/G | 1.64738e-05 | 0.00286995 | missense | CFAP52 | GRCh38.p7 | 17:9635447 | ACCCAGAAGCTGGAG[A/G]AGGCCCTGAAGGAAC | 146845 |
| rs749851247 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9597455 | CTACAATGTGTATAT[A/G]TATATAAACATCATG | 146845 |
| rs749896157 | in-del | -/TTTG | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9600554 | GGACAAAGCACACAC[-/TTTG]TTTGTTTGTTTGTTT | 146845 |
| rs749903765 | in-del | -/GAGT | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9586549 | AGCCTGGGCAAAAAA[-/GAGT]GAGACTCCGTCTCAA | 146845 |
| rs749905907 | snp | C/T | 1.69223e-05 | 0.00290876 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586687 | ATCTGACGGTGTGTT[C/T]TTGCCCCCAGGCAGA | 146845 |
| rs749947245 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636089 | TGAGGCAGGAGAGTC[A/G]CTTGAACCCAGGATG | 146845 |
| rs749965991 | snp | C/G | 1.98285e-05 | 0.00314863 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642990 | CTCTCTCTCCTATTG[C/G]AGCAATGCCATATAC | 146845 |
| rs750059856 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9638042 | TTTTGGGACATCCCC[A/C]CGTGACAGGCTCGTG | 146845 |
| rs750092026 | snp | C/T | 3.43389e-05 | 0.00414346 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598198 | TTAAATGGGTGTCCA[C/T]TTGATTGTGGTTTTT | 146845 |
| rs750092965 | snp | C/T | 3.2994e-05 | 0.00406152 | missense, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643080 | GTGAAGTGACTCACG[C/T]TGGGGTGGGACACAG | 146845 |
| rs750140952 | snp | A/C | | | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9577126 | CGCCGCTCGCAAAGC[A/C]CTAGGCTCCTTCGTA | 146845 |
| rs750210555 | snp | A/C | 1.64738e-05 | 0.00286995 | missense | CFAP52 | GRCh38.p7 | 17:9635435 | ATAGGCTGTCAGACC[A/C]AGAAGCTGGAGGAGG | 146845 |
| rs750220831 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9607920 | ACATCCTCCAGGCAA[C/T]GTGTGCAGCACTGGC | 146845 |
| rs750298569 | snp | A/G | 3.33467e-05 | 0.00408316 | splice-acceptor-variant | CFAP52 | GRCh38.p7 | 17:9608117 | ACAGTTTTTCCCCCT[A/G]GGGAGTGTCAGCTAT | 146845 |
| rs750347246 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9628051 | AATAAAGTAGTTTTA[C/T]AGAAAAGACAAATGT | 146845 |
| rs750390388 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9587719 | TAATGGAGTTTTTGT[C/T]TTATCTTATAAATTT | 146845 |
| rs750409926 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9640559 | CTCCATCCATGTCCC[A/G]GCAAAGGACATGATC | 146845 |
| rs750491859 | snp | C/T | 3.29516e-05 | 0.00405891 | missense | CFAP52 | GRCh38.p7 | 17:9612370 | GAAGGACACCAGTTT[C/T]TCGTAGGAACAGAAG | 146845 |
| rs750540153 | snp | A/T | 1.6676e-05 | 0.00288751 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638733 | CCTCCCAGTGAGAGA[A/T]GAGATCTTTCCAGCG | 146845 |
| rs750593072 | snp | C/T | 1.64789e-05 | 0.0028704 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9612432 | TTTCAAAGAGACGCT[C/T]ATAGCGACTTGTCAC | 146845 |
| rs750657371 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9613640 | CTCCTGCCTCAGCCT[C/T]CTGAGTAGCTAGGAT | 146845 |
| rs750684088 | snp | A/G | 1.66966e-05 | 0.00288929 | synonymous-codon, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643174 | TGGAGCCATTTTGCG[A/G]TGGAAGTACCCATAT | 146845 |
| rs750736659 | snp | C/G | 3.31257e-05 | 0.00406962 | splice-acceptor-variant | CFAP52 | GRCh38.p7 | 17:9594192 | CCTCTTATTTTGGCA[C/G]TGTGGTGGTGTGGAG | 146845 |
| rs750744776 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9582003 | TGCCAGTTGTGTGAG[C/T]AATATGTATTCCTTC | 146845 |
| rs750744883 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9590689 | ACTAGGTCTTGCGGG[A/G]AAAATGGCCCCTTAA | 146845 |
| rs750820182 | in-del | -/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9580688 | AGTGAGACCTGGTCT[-/C]AAAAAAAAAAAAAAA | 146845 |
| rs750835772 | snp | C/T | 1.67626e-05 | 0.002895 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9598270 | ATTGGATCTTCCAAA[C/T]AGAAAAATCTGGCCA | 146845 |
| rs750929629 | snp | A/T | 1.64727e-05 | 0.00286986 | splice-donor-variant | CFAP52 | GRCh38.p7 | 17:9635558 | ATTTGGGACCTTGTG[A/T]AGGTACCTGTGATGG | 146845 |
| rs750934625 | snp | C/T | 1.64819e-05 | 0.00287066 | missense | CFAP52 | GRCh38.p7 | 17:9638635 | GGAATCAGATGATAC[C/T]AGCCAACACCTTATT | 146845 |
| rs750954649 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9606028 | GGAAATCTCAAATAC[C/T]TGTATCTTCTGTTTA | 146845 |
| rs750987599 | in-del | -/ATAACAT | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9610152 | CAGGAGAGGAAAGAA[-/ATAACAT]ATAACATCCAAGTAT | 146845 |
| rs751028010 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9594144 | TTTCTTATTTTAAAA[C/G]CCTGTTTTCTCTTTG | 146845 |
| rs751102367 | snp | C/G | 1.64852e-05 | 0.00287094 | missense | CFAP52 | GRCh38.p7 | 17:9632929 | TTCGCCCCAGAGACA[C/G]GCCGACTGATGTATG | 146845 |
| rs751137597 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631581 | TTGGTGGATTTGAGG[A/G]ATAGCAAGAGGGCCA | 146845 |
| rs751216569 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9627838 | AGATCTTCCTTCCTC[A/G]GCCTCCTAAGAAGCC | 146845 |
| rs751236131 | snp | C/T | | | upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9575965 | TATAATCAGAGAAAG[C/T]AAAGCGCTCCCCTGC | 146845 |
| rs751311669 | snp | A/G | 3.32226e-05 | 0.00407556 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600031 | CAGGCGTGAGCCACC[A/G]AGGCTGGCCAAGATT | 146845 |
| rs751326025 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576928 | GCACAGCCTGACCTG[C/T]CCCAAGGCCTTGGAG | 146845 |
| rs751337737 | snp | C/G | 1.68806e-05 | 0.00290517 | intron-variant | CFAP52 | GRCh38.p7 | 17:9608227 | CCCATCAAGTAAGTT[C/G]CGGGTCTCACACAGT | 146845 |
| rs751364192 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9626642 | GCTCATTCACCAAAG[G/T]CATTATCTAATATAA | 146845 |
| rs751394782 | snp | C/G | 1.65285e-05 | 0.00287471 | missense | CFAP52 | GRCh38.p7 | 17:9586731 | GATTATAAGAACAGA[C/G]AGCTGCTTGCTCGGC | 146845 |
| rs751435752 | snp | C/T | 1.86967e-05 | 0.00305745 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643003 | TGCAGCAATGCCATA[C/T]ACGTGTTTATCTTTT | 146845 |
| rs751546741 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9585633 | CCCAAGACTGCACCA[C/T]TGCACCCCAGGCTGG | 146845 |
| rs751551727 | snp | G/T | 1.6483e-05 | 0.00287076 | missense, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643104 | GACACAGTGGCAACA[G/T]CACACGCATCCGCAT | 146845 |
| rs751568398 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9600604 | GAGTCTCGCTCTGTC[A/G]CCCAGGCTGGCGTGC | 146845 |
| rs751576882 | snp | A/G | 1.67472e-05 | 0.00289367 | missense | CFAP52 | GRCh38.p7 | 17:9586834 | GCCCAGATGACGGAA[A/G]GTAATGAACTAAACA | 146845 |
| rs751624199 | snp | A/C | 1.65045e-05 | 0.00287263 | missense | CFAP52 | GRCh38.p7 | 17:9594213 | TGGTGTGGAGCATAG[A/C]CAAGAGAGATGCCAT | 146845 |
| rs751688968 | snp | A/T | 1.76042e-05 | 0.00296678 | intron-variant | CFAP52 | GRCh38.p7 | 17:9628645 | CTGCATCTTTTATGG[A/T]TGCATCTCTTGATGG | 146845 |
| rs751706021 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9591532 | GATGTGCTGGAATCT[A/G]TTTGGCCAGATCTCT | 146845 |
| rs751826661 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9590261 | ACCTATGCCCATGTG[C/T]CTGCCCTTCTGGCGG | 146845 |
| rs751871126 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9592653 | CTTCTTTCACTTAGC[A/G]TAATGTTTTCAAAGT | 146845 |
| rs751894245 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9613302 | CCAGCAGTTTTGATA[C/T]CAAAAGGAGCTTCAG | 146845 |
| rs751919994 | snp | C/T | 3.29462e-05 | 0.00405857 | intron-variant, missense | CFAP52 | GRCh38.p7 | 17:9585829 | CATATGATTTATCCT[C/T]TTGGTTGCACAGTCC | 146845 |
| rs751932875 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9603855 | AAAAAAAGAAAGCAC[A/T]ATATTGAAGAAGAAC | 146845 |
| rs751937898 | snp | C/T | 0.000148315 | 0.00861021 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9638645 | GATACTAGCCAACAC[C/T]TTATTCCAGTGTGTG | 146845 |
| rs751958256 | in-del | -/GAC | 3.3355e-05 | 0.00408367 | cds-indel, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576744 | GCGGAGCTGGAACTT[-/GAC]GCCGTGATCGGCTTC | 146845 |
| rs752010250 | in-del | -/TG | 1.65943e-05 | 0.00288043 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600035 | GTGAGCCACCGAGGC[-/TG]TGGCCAAGATTTCTT | 146845 |
| rs752026624 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9585391 | TTTAAAGTGTTGGCC[A/G]GGCGCGGTGGCTCAC | 146845 |
| rs752053191 | snp | G/T | 3.34599e-05 | 0.00409009 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638742 | GAGAGATGAGATCTT[G/T]CCAGCGCAAGAGAAA | 146845 |
| rs752058115 | snp | A/G | 3.29582e-05 | 0.00405931 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9612438 | AGAGACGCTCATAGC[A/G]ACTTGTCACTTTGAT | 146845 |
| rs752070886 | in-del | -/A | | | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641533 | ATAGAATGCAAATTT[-/A]AAAACCAATACTAAA | 146845 |
| rs752105535 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636938 | TTATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 146845 |
| rs752115867 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9592299 | GAAACCCTGTCTCTA[C/T]TAAAAATGCAAAAAA | 146845 |
| rs752178735 | snp | A/G | 3.32276e-05 | 0.00407586 | missense | CFAP52 | GRCh38.p7 | 17:9633019 | AGGGTCATCAGTGGC[A/G]GTGGGGAAGGGGAGG | 146845 |
| rs752233727 | snp | G/T | 4.94181e-05 | 0.00497057 | missense | CFAP52 | GRCh38.p7 | 17:9600163 | ACAGATGTTGGGCCT[G/T]CGAAGGACAAATTCA | 146845 |
| rs752278009 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9638174 | TGATTAAAACATAAA[A/C]AAAATAAAATACCCT | 146845 |
| rs752279976 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9625621 | TGCCACCTTTTTCTA[C/T]AGCCACCATAGCTGT | 146845 |
| rs752308451 | in-del | -/A | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9639630 | CCAATCCATGAATGG[-/A]CAATGAATAACAAGT | 146845 |
| rs752343786 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9584393 | ACTCAGAACTGAAAC[C/T]GAAAGTTAAAAAAAT | 146845 |
| rs752369966 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9626497 | GGCCTCCCAAAGCAC[C/T]GGGATTACAGGCATG | 146845 |
| rs752434292 | in-del | -/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9593222 | CCCCAGCATTTTTTT[-/G]TATTATGATCCACAC | 146845 |
| rs752464308 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9586156 | GGACTCTGATGATTT[C/T]ATACCCGAGGTTGCA | 146845 |
| rs752505017 | snp | C/T | 3.29641e-05 | 0.00405968 | missense, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643109 | AGTGGCAACATCACA[C/T]GCATCCGCATAAGTC | 146845 |
| rs752552784 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9597251 | AATTTCTTCCCATTG[C/T]GTACATATACCACAT | 146845 |
| rs752605017 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9634712 | GAGGTCGCAGTGAGC[C/T]GAGATCGCGCCATTG | 146845 |
| rs752629234 | snp | A/G | 1.65548e-05 | 0.002877 | missense, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643160 | AGTGTAAGTGCCGAT[A/G]GAGCCATTTTGCGAT | 146845 |
| rs752681211 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9610608 | GACGCCATCTTGGCT[C/T]ACTGCAACCTCCGCC | 146845 |
| rs752697039 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631123 | ACATAAGTCAGAATT[C/T]GCCATATTTAGGGCT | 146845 |
| rs752727251 | snp | C/G | 1.6483e-05 | 0.00287076 | missense | CFAP52 | GRCh38.p7 | 17:9632935 | CCAGAGACAGGCCGA[C/G]TGATGTATGTCATTA | 146845 |
| rs752733752 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9578081 | TGGGGGACAGAGCGA[C/G]ACTCCGTCTCAAAAA | 146845 |
| rs752780108 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9600355 | CAAGCGATTGTCCCA[C/T]CTCAGCCTCTCAAGT | 146845 |
| rs752819814 | in-del | -/G | 0.000131774 | 0.00811601 | frameshift-variant | CFAP52 | GRCh38.p7 | 17:9600134 | TAAAAATGAACCCCA[-/G]GACTAAACTGCTGAC | 146845 |
| rs752851311 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9603118 | CCTAGCACTTGGGAA[C/T]GAAATATCTGTCCAG | 146845 |
| rs752873225 | in-del | -/A | 1.64834e-05 | 0.00287079 | intron-variant, frameshift-variant | CFAP52 | GRCh38.p7 | 17:9585930 | CATCTCCAGGTCTGG[-/A]GAGTACATCGCCTCC | 146845 |
| rs752874173 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631189 | GATCCCCCCATCACC[C/T]ACAAGGCTCCATGTG | 146845 |
| rs752879145 | in-del | -/AA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636241 | AGAAAGAAAGAAAGA[-/AA]GAAAGAAAGAGAAAG | 146845 |
| rs752953359 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9613079 | CTTAGGATATTTTCA[A/G]TTACATTGGGTTTAT | 146845 |
| rs753129964 | snp | G/T | 1.64781e-05 | 0.00287033 | missense, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641772 | ATCAGAGAATTGGAA[G/T]GTTCCCTGTCTGGGT | 146845 |
| rs753179512 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9594821 | AGAGGCCAGTATCTG[C/T]CTAAGGGAGGGAATA | 146845 |
| rs753191915 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9635156 | TGATTAAATTTCTCA[A/G]CCTGTATGTACAAGC | 146845 |
| rs753256974 | snp | C/T | 3.29571e-05 | 0.00405924 | missense | CFAP52 | GRCh38.p7 | 17:9594285 | CCAATGTGATCTTCT[C/T]CAGGTGCCGGGATGA | 146845 |
| rs753283857 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9615346 | ATTACAGAGACGTGC[A/G]TTGCAGCAAAAGAGA | 146845 |
| rs753342880 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9638082 | GGTTGTGCATGATAT[A/G]GTACGTCCAAACCTG | 146845 |
| rs753377994 | snp | G/T | 1.77225e-05 | 0.00297673 | intron-variant | CFAP52 | GRCh38.p7 | 17:9608082 | TGGTGATTTGTGAGA[G/T]TTTTGTGCTTTTTCT | 146845 |
| rs753378334 | snp | C/G | 1.65644e-05 | 0.00287783 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585982 | TTCAAGGTGAATACA[C/G]TGAAAACGACTCATT | 146845 |
| rs753420889 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636328 | CAGAATGAACTTCCC[A/G]TGGAGGGGAGGGATG | 146845 |
| rs753422223 | snp | A/C | 1.64814e-05 | 0.00287061 | intron-variant, synonymous-codon | CFAP52 | GRCh38.p7 | 17:9585922 | TGCTTGGCCATCTCC[A/C]GGTCTGGAGAGTACA | 146845 |
| rs753441871 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9598618 | AATACACAAGTAGCC[A/C]GGTGTGGTGGTAGGT | 146845 |
| rs753442442 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9620902 | AACCATAAAAACCCT[A/G]GAAGAAAACCTAGGC | 146845 |
| rs753612636 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9603243 | ATACAGAGTCTCGCT[C/G]TGTCGCCCAGGCTGG | 146845 |
| rs753618468 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9595764 | TGACATGGCACCTAT[A/G]TATGCTGGGTTCTCT | 146845 |
| rs753655355 | snp | A/G | 1.64901e-05 | 0.00287137 | missense | CFAP52 | GRCh38.p7 | 17:9632962 | ATTAACAATGCTCAC[A/G]GGATCGGCGTCACCG | 146845 |
| rs753753880 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9588684 | CCATTCAGTGTGATA[A/G]TTTGCTGTGGGTTTG | 146845 |
| rs753775549 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9577226 | GCGTACCAGTGAGAA[A/G]GGGCTGGGAGGGAAC | 146845 |
| rs753776498 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9578009 | AGGGAGGAGAATCAC[C/T]TGAACTTGGGAGGCA | 146845 |
| rs753851171 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9608921 | GTCACTACCAGACAA[A/G]ATAGGATATTAGCAC | 146845 |
| rs753878173 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9587755 | AGTTCTGTATAGATG[C/T]AAGATACTTTTTCAG | 146845 |
| rs753905234 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9630566 | TCCCGAGTAGCTGGG[A/G]CTACAGGCGCCCGCT | 146845 |
| rs753941100 | in-del | -/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9591231 | TAGTAGAGACGGGGG[-/T]CTCTTCATGTTGGTC | 146845 |
| rs753969601 | in-del | -/T | 1.70095e-05 | 0.00291625 | intron-variant | CFAP52 | GRCh38.p7 | 17:9608106 | TTTTTCTTAACACAG[-/T]TTTTCCCCCTAGGGA | 146845 |
| rs753993075 | snp | A/G/T | 1.6489e-05 | 0.00287128 | missense | CFAP52 | GRCh38.p7 | 17:9635538 | GCACCGATGGGACTT[A/G/T]TATCATTTGGGACCT | 146845 |
| rs754002991 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9615191 | TAATGTTCTTTGTTT[C/T]CAATTGCTATTACTT | 146845 |
| rs754039656 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9640171 | ACATGAAACAATGAG[A/T]AACAAATGAAATGCA | 146845 |
| rs754046396 | snp | A/T | 1.64963e-05 | 0.00287192 | missense | CFAP52 | GRCh38.p7 | 17:9638614 | TACTTTCCAGGCGTC[A/T]CAGGAGGAATCAGAT | 146845 |
| rs754143724 | snp | C/T | 1.6507e-05 | 0.00287284 | missense | CFAP52 | GRCh38.p7 | 17:9586741 | ACAGAGAGCTGCTTG[C/T]TCGGCTGTCCCTTCA | 146845 |
| rs754169117 | snp | A/G | 1.64751e-05 | 0.00287007 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9612360 | ACTTCGAGGAGAAGG[A/G]CACCAGTTTCTCGTA | 146845 |
| rs754207909 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9582358 | CATTTTGGTGGATAT[G/T]ACATGGTATCTCATT | 146845 |
| rs754259989 | snp | A/C | 0.000132059 | 0.00812478 | missense | CFAP52 | GRCh38.p7 | 17:9628772 | ACCGTGCCCAACATG[A/C]CCTGCCACGGCATCG | 146845 |
| rs754278144 | snp | A/G | 1.72142e-05 | 0.00293374 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598190 | AGTGATTATTAAATG[A/G]GTGTCCATTTGATTG | 146845 |
| rs754287718 | snp | A/C | | | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575427 | TGACATGCTACAAAA[A/C]CGTTATTTCGACTTC | 146845 |
| rs754291097 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9593094 | ATAATACATTCCATA[C/T]GTAGAAAAGTTGGGA | 146845 |
| rs754292439 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9585589 | AGCAGGAGAATCACT[G/T]GAACCCAGGAGGTGA | 146845 |
| rs754400931 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9633841 | GCCACCACGCCCAGC[G/T]AATTTTTTTTTGTAT | 146845 |
| rs754402594 | snp | C/T | 1.6782e-05 | 0.00289668 | missense | CFAP52 | GRCh38.p7 | 17:9598262 | GTATGGGAATTGGAT[C/T]TTCCAAATAGAAAAA | 146845 |
| rs754403920 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9581144 | ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 146845 |
| rs754404537 | snp | A/C/G | 3.33007e-05 | 0.00408038 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | CFAP52, STX8 | GRCh38.p7 | 17:9576731 | GGAGGCCCAAGTGGC[A/C/G]GAGCTGGAACTTGAC | 146845 |
| rs754520869 | snp | C/G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9603266 | CAGGCTGGAGTGCAG[C/G/T]GGCACTATCTCGGCT | 146845 |
| rs754523247 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9604693 | GAATCACTTGAACCC[A/G]GCAGTGAGATCACGC | 146845 |
| rs754541732 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642484 | CAAAAATTAGCCGGG[C/T]GTGGTGGTGCACGCC | 146845 |
| rs754544781 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9623614 | TTCATTCTTTCTTAT[A/G]TATCTAAGTTGTCAT | 146845 |
| rs754555801 | snp | C/T | | | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575030 | GTTATAGAGCTGTAA[C/T]ATGTTTTTAATTATT | 146845 |
| rs754600270 | snp | A/G | 1.67248e-05 | 0.00289173 | missense | CFAP52 | GRCh38.p7 | 17:9598301 | ACTGAGTGCCAAACA[A/G]GACAGTTGAAAAGAA | 146845 |
| rs754679466 | snp | C/T | 8.32341e-05 | 0.00645059 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586005 | GACTCATTGTCAATT[C/T]ATCTAGAGGTGCCTC | 146845 |
| rs754733950 | in-del | -/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9637662 | TCACTGCAGCCTCTG[-/C]CTCCCGGGTTCAAGT | 146845 |
| rs754782651 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9596261 | CATGCTGCCACGCCC[A/G]GCTAATTTTTTTGTA | 146845 |
| rs754850821 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9578012 | GAGGAGAATCACTTG[A/C]ACTTGGGAGGCAGAG | 146845 |
| rs754906690 | snp | C/G | 1.6483e-05 | 0.00287076 | missense, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643105 | ACACAGTGGCAACAT[C/G]ACACGCATCCGCATA | 146845 |
| rs754928198 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9609002 | GAGGATGACCTTCTC[A/G]GGATGGAAAGATCAG | 146845 |
| rs755007602 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9596870 | ACAGGTGCCCACCAC[C/T]ACGCCTGGCTAATTT | 146845 |
| rs755014033 | snp | C/T | 1.64773e-05 | 0.00287026 | missense | CFAP52 | GRCh38.p7 | 17:9594276 | GCAATGCCACCAATG[C/T]GATCTTCTCCAGGTG | 146845 |
| rs755039224 | snp | C/T | 3.30044e-05 | 0.00406216 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9594214 | GGTGTGGAGCATAGC[C/T]AAGAGAGATGCCATC | 146845 |
| rs755071760 | in-del | -/AG | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9597805 | GACTCTGTCAGAAAG[-/AG]AGAGAGAGAGAGAGA | 146845 |
| rs755094177 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9628486 | GGTTTCACCATGTTG[A/G]TCAGGCTGGTCTCAA | 146845 |
| rs755140430 | snp | C/T | 2.22378e-05 | 0.00333443 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575848 | GACTCTTCCTGCTCT[C/T]AGCAGCTGACTACGG | 146845 |
| rs755174612 | in-del | -/TCT | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9591231 | TAGTAGAGACGGGGG[-/TCT]CTTCATGTTGGTCAG | 146845 |
| rs755260034 | in-del | -/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9632077 | TGCGCCCAGCCTCCA[-/C]TTTTTTTTTTCTTTT | 146845 |
| rs755272669 | snp | A/G | 1.64811e-05 | 0.00287059 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9638654 | CAACACCTTATTCCA[A/G]TGTGTGTGCTATCAC | 146845 |
| rs755323731 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9611087 | AACTTGTCATCTTCC[C/T]TTCGTCATTAACTGT | 146845 |
| rs755344420 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9600619 | GCCCAGGCTGGCGTG[C/T]AGTGGCGAGATGTCG | 146845 |
| rs755353746 | snp | A/C/G | 4.94192e-05 | 0.00497067 | intron-variant, missense | CFAP52 | GRCh38.p7 | 17:9585832 | ATGATTTATCCTCTT[A/C/G]GTTGCACAGTCCTCA | 146845 |
| rs755376369 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9615194 | TGTTCTTTGTTTTCA[A/G]TTGCTATTACTTTAT | 146845 |
| rs755450527 | snp | C/G | 1.64795e-05 | 0.00287045 | missense | CFAP52 | GRCh38.p7 | 17:9612440 | AGACGCTCATAGCGA[C/G]TTGTCACTTTGATGC | 146845 |
| rs755456447 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9581168 | AAAAATACCAAAAAA[A/T]TAGCCGGGCGCGGTG | 146845 |
| rs755544513 | in-del | -/A | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636198 | AAAGAAAGAAAGAAA[-/A]GAAAGAAAGAAAGAA | 146845 |
| rs755670801 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9586635 | TTTCACCAAGAAGGG[C/T]AGCTATCTCCTCAGA | 146845 |
| rs755686536 | snp | A/C | 1.64732e-05 | 0.0028699 | intron-variant, missense | CFAP52 | GRCh38.p7 | 17:9585847 | GGTTGCACAGTCCTC[A/C]TTCAGGCAATAAATA | 146845 |
| rs755791398 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9584112 | GATGCCATCTGCCCT[G/T]TTCTTACCAGGCTGG | 146845 |
| rs755824895 | snp | A/G | 1.68995e-05 | 0.00290679 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638754 | CTTTCCAGCGCAAGA[A/G]AAAAGCAGTGAGGCG | 146845 |
| rs755926528 | snp | A/C | 0.000190402 | 0.00975524 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586847 | AAGGTAATGAACTAA[A/C]CATAGTTACTTATTT | 146845 |
| rs755948997 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9629200 | TCAAAGGGAATTTAT[G/T]TTTAACTCAATTTAT | 146845 |
| rs755950705 | snp | C/T | | | upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576292 | GCTCCAAACAGGGGC[C/T]CAAAGAAGTATCAAT | 146845 |
| rs755961824 | snp | C/T | 5.0048e-05 | 0.00500215 | stop-gained, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643172 | GATGGAGCCATTTTG[C/T]GATGGAAGTACCCAT | 146845 |
| rs755972760 | snp | C/T | 1.64855e-05 | 0.00287097 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9632952 | GATGTATGTCATTAA[C/T]AATGCTCACAGGATC | 146845 |
| rs755992736 | snp | A/T | 6.69333e-05 | 0.00578465 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632873 | TGCCTGCCTTTTGTT[A/T]CCCTTTCATGCCAGC | 146845 |
| rs756043856 | snp | G/T | 1.6729e-05 | 0.00289209 | missense | CFAP52 | GRCh38.p7 | 17:9598314 | CAGGACAGTTGAAAA[G/T]AATAGTCATGAGTAT | 146845 |
| rs756073774 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9628419 | TGAGTAGCTGGGATT[A/G]CAGGCATGCACCACC | 146845 |
| rs756095656 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9577149 | CCTTCGTAACCACAC[A/G]GAAGGATGCTGTCTG | 146845 |
| rs756159401 | snp | C/G | 1.6649e-05 | 0.00288518 | missense, upstream-variant-2KB, utr-variant-5-prime | CFAP52, STX8 | GRCh38.p7 | 17:9576723 | ATTTCGCCGGAGGCC[C/G]AAGTGGCGGAGCTGG | 146845 |
| rs756205458 | in-del | -/AA | 1.6473e-05 | 0.00286988 | frameshift-variant | CFAP52 | GRCh38.p7 | 17:9600158 | GCTGACAGATGTTGG[-/AA]GCCTGCGAAGGACAA | 146845 |
| rs756257397 | snp | C/T | 1.65356e-05 | 0.00287533 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9608139 | GTCAGCTATCAGGTG[C/T]CTGAAGATGGGGGGT | 146845 |
| rs756260777 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9638591 | TCGACTTTCACAGCT[G/T]TTGAATCTACTTTCC | 146845 |
| rs756298941 | in-del | -/T/TT | 0.157758 | 0.232635 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598215 | GATTGTGGTTTTTTG[-/T/TT]TTTTTTTTTTTTACA | 146845 |
| rs756316028 | snp | A/C/G | 4.94208e-05 | 0.00497075 | missense | CFAP52 | GRCh38.p7 | 17:9635445 | AGACCCAGAAGCTGG[A/C/G]GGAGGCCCTGAAGGA | 146845 |
| rs756371024 | snp | C/T | 6.59163e-05 | 0.00574054 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9635527 | TGTCACCGCCAGCAC[C/T]GATGGGACTTGTATC | 146845 |
| rs756391328 | in-del | -/GATGCTTTTAATGCCTCCCTATGATCT | 1.70895e-05 | 0.00292309 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586649 | GTAGCTATCTCCTCA[-/GATGCTTTTAATGCCTCCCTATGATCT]GACGGTGTGTTCTTG | 146845 |
| rs756395700 | in-del | -/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9601863 | TCTCGTTTCTGATAA[-/C]AGAACAGATGGTTCT | 146845 |
| rs756482110 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9606831 | TGAGGCACTTAGGAA[C/G]TTAGGGGTGAGGGGT | 146845 |
| rs756520413 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9579724 | AGGTATCCACCACCA[A/C]GCCTGGCTAATTTTT | 146845 |
| rs756537922 | snp | A/G | 1.64819e-05 | 0.00287066 | missense | CFAP52 | GRCh38.p7 | 17:9594237 | ATGCCATCTGTGGCA[A/G]CCCTGCAGCCGGCCT | 146845 |
| rs756541535 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9608717 | TATGTATGTTTCTTG[A/G]CTCATTTAATTAAAA | 146845 |
| rs756574575 | snp | C/T | | | intron-variant, missense | CFAP52 | GRCh38.p7 | 17:9585934 | TCCAGGTCTGGAGAG[C/T]ACATCGCCTCCGGAC | 146845 |
| rs756591205 | snp | G/T | 1.64798e-05 | 0.00287047 | missense | CFAP52 | GRCh38.p7 | 17:9594288 | ATGTGATCTTCTCCA[G/T]GTGCCGGGATGAGAT | 146845 |
| rs756608101 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9581029 | AGAAGTTTTAAAAAA[C/T]TACGTGGCCAGGCGT | 146845 |
| rs756635004 | in-del | -/A | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9580690 | TGAGACCTGGTCTCA[-/A]AAAAAAAAAAAAAAT | 146845 |
| rs756723519 | in-del | -/TGT | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9622416 | TAAATAAACTGGACA[-/TGT]TGGTGGCACTGCCTC | 146845 |
| rs756761544 | snp | A/G | 5.12597e-05 | 0.00506233 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641690 | TGACTCTCCTGAGCT[A/G]AGTCCTGCTTAATGC | 146845 |
| rs756817615 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9595003 | TCAAGCAATTCTCCT[A/G]CCTCAGCCTCCCAAG | 146845 |
| rs756825001 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9634243 | TAGGAAGAACAGAAT[A/G]GTTTGTGCTCATCTT | 146845 |
| rs756833478 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9620912 | ACCCTAGAAGAAAAC[C/T]TAGGCATTACCGTTC | 146845 |
| rs756845036 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9635182 | CAAGCAGGTACAGGA[C/T]TGTTAGTAGCATTTT | 146845 |
| rs756848777 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9582791 | ATAGGTGTCCACCAC[G/T]ACGCCCAGCTAATTT | 146845 |
| rs756886009 | snp | C/T | 3.29565e-05 | 0.00405921 | missense, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641788 | GTTCCCTGTCTGGGT[C/T]GATAAATGGCATGGA | 146845 |
| rs756891499 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631672 | TTAAAAGAGATGGCG[C/G]GGGTTGGGGGTCGGG | 146845 |
| rs756901981 | snp | C/T | 1.65886e-05 | 0.00287993 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9628696 | TGAGCTATTTGCAAC[C/T]TGTGCCAAGAAGGAT | 146845 |
| rs756917905 | in-del | -/AAAT | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9578098 | TCCGTCTCAAAAAAT[-/AAAT]AAATAAATAAATAAA | 146845 |
| rs756980914 | snp | C/T | 1.64912e-05 | 0.00287147 | missense | CFAP52 | GRCh38.p7 | 17:9632966 | ACAATGCTCACAGGA[C/T]CGGCGTCACCGCCAT | 146845 |
| rs757003127 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9627896 | CAGCTAATTTTTATA[C/T]ATTTTTATTTTTTGG | 146845 |
| rs757036325 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9600610 | CGCTCTGTCGCCCAG[A/G]CTGGCGTGCAGTGGC | 146845 |
| rs757052324 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9606457 | GCTGATGTGTCAGAC[A/G]TGGTGCAAAACCCCT | 146845 |
| rs757065743 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9626828 | CCCCAAGCATTAAAT[A/G]TGTGGAAGGGATCCA | 146845 |
| rs757101908 | snp | G/T | 3.40826e-05 | 0.00412797 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633052 | TTGAAAGCAGAAATT[G/T]GAAAAAATAACGCTC | 146845 |
| rs757103807 | snp | A/T | 1.64776e-05 | 0.00287028 | missense | CFAP52 | GRCh38.p7 | 17:9600085 | GATGATGATGATAGC[A/T]TTTTCTACCTTGGCA | 146845 |
| rs757131819 | in-del | -/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9634339 | TGTAGTTGTGACAGA[-/T]CCTTTGTCCATTAAA | 146845 |
| rs757155125 | snp | A/T | 1.64743e-05 | 0.00287 | missense | CFAP52 | GRCh38.p7 | 17:9600176 | CTGCGAAGGACAAAT[A/T]CAGTTTGGTGAGTAG | 146845 |
| rs757255815 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9638363 | CTGTCTTTAGGAAAG[G/T]GCCCTTCCCATTGTC | 146845 |
| rs757258446 | snp | A/G | | | missense | CFAP52 | GRCh38.p7 | 17:9612353 | CTATCACACTTCGAG[A/G]AGAAGGACACCAGTT | 146845 |
| rs757284112 | snp | A/G | | | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575347 | GGTTACTAACTGGCT[A/G]GTGGCCATGGATTCT | 146845 |
| rs757291790 | snp | A/G | 0.000109427 | 0.00739605 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584332 | TTGCCTGTGGAAAGA[A/G]GTGTCACCATGAAAG | 146845 |
| rs757303109 | snp | C/G | 1.64727e-05 | 0.00286986 | missense | CFAP52 | GRCh38.p7 | 17:9635555 | ATCATTTGGGACCTT[C/G]TGTAGGTACCTGTGA | 146845 |
| rs757446071 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9579594 | TGTTTTTGAGATGGA[A/G]TCTCACCCTGTCTCC | 146845 |
| rs757485213 | in-del | -/TTTGT | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9623691 | TTGTTTGTTTGTTTG[-/TTTGT]TTGTTTAAGAGACAG | 146845 |
| rs757506984 | snp | C/T | 1.64798e-05 | 0.00287047 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9628780 | CAACATGACCTGCCA[C/T]GGCATCGACTTCATG | 146845 |
| rs757527507 | snp | C/T | 4.95176e-05 | 0.00497558 | missense | CFAP52 | GRCh38.p7 | 17:9586743 | AGAGAGCTGCTTGCT[C/T]GGCTGTCCCTTCACA | 146845 |
| rs757540782 | in-del | -/G | 1.65239e-05 | 0.00287431 | frameshift-variant | CFAP52 | GRCh38.p7 | 17:9608148 | CAGGTGCCTGAAGAT[-/G]GGGGGTTTGTTGGTG | 146845 |
| rs757590710 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9622425 | TGGACATGTTGGTGG[C/T]ACTGCCTCTAGTCCC | 146845 |
| rs757616996 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642341 | ATTAACAAATAAATG[C/T]GGCCAGGCGTGGTGG | 146845 |
| rs757618576 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9639200 | TTTGTGAGGCTGAGG[C/T]GGGTGGATCACCTGA | 146845 |
| rs757630300 | snp | A/G | 6.88314e-05 | 0.00586609 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598191 | GTGATTATTAAATGG[A/G]TGTCCATTTGATTGT | 146845 |
| rs757659050 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9590273 | GTGCCTGCCCTTCTG[A/G]CGGGCCAAGGTGTTT | 146845 |
| rs757660482 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9603931 | ACTACAGTAATCAAG[A/G]CAGTGTAGGGTTGGT | 146845 |
| rs757789260 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9603365 | AGGCGCCTACCACCA[G/T]GCCCAGCTAACTTTT | 146845 |
| rs757886482 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9606225 | TATTTCTGTGAAAAG[C/T]TTTTAAAAATTAGCC | 146845 |
| rs757913515 | snp | C/T | 3.91106e-05 | 0.00442197 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642993 | TCTCTCCTATTGCAG[C/T]AATGCCATATACGTG | 146845 |
| rs757930429 | snp | A/G | | | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575154 | CAGTCCTTGGGATTA[A/G]CTGCTAAATAAATCA | 146845 |
| rs757994347 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9593163 | AACATTTTCATTCTT[G/T]TTCTTTAAACACCTT | 146845 |
| rs758095633 | snp | A/T | 1.65935e-05 | 0.00288036 | intron-variant | CFAP52 | GRCh38.p7 | 17:9628871 | TAGCTGCGGTTTTGA[A/T]TCTTGTCACTCTCCT | 146845 |
| rs758135975 | snp | A/G | 1.64757e-05 | 0.00287012 | splice-donor-variant | CFAP52 | GRCh38.p7 | 17:9600184 | GACAAATTCAGTTTG[A/G]TGAGTAGAGACCATC | 146845 |
| rs758139114 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9638269 | GTACATTGTGTGGGA[C/G]GCAGCAGGTTGGCTG | 146845 |
| rs758150811 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9584462 | AGGTTGTATCAATTT[A/G]AAGTGTATAACACAA | 146845 |
| rs758157956 | snp | C/G/T | 3.29474e-05 | 0.00405867 | missense, synonymous-codon | CFAP52 | GRCh38.p7 | 17:9635441 | TGTCAGACCCAGAAG[C/G/T]TGGAGGAGGCCCTGA | 146845 |
| rs758206948 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9637233 | GGTTCAAGGACCACA[C/T]TTGTAGGAAGTGTTA | 146845 |
| rs758236820 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9585409 | CGCGGTGGCTCACAC[C/T]TGTAATCCCAGCACT | 146845 |
| rs758238677 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9598848 | GACACAGCACAGGTA[A/G]ACCTTGTTTTGCTGG | 146845 |
| rs758256764 | snp | A/G | 1.64846e-05 | 0.0028709 | intron-variant, synonymous-codon | CFAP52 | GRCh38.p7 | 17:9585930 | CATCTCCAGGTCTGG[A/G]GAGTACATCGCCTCC | 146845 |
| rs758263833 | in-del | -/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9629548 | TCCTTGCTTGCTTGC[-/T]TTTTTTTTTTTTTTC | 146845 |
| rs758282672 | snp | A/G | 1.66396e-05 | 0.00288436 | missense | CFAP52 | GRCh38.p7 | 17:9608119 | AGTTTTTCCCCCTAG[A/G]GAGTGTCAGCTATCA | 146845 |
| rs758309454 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9612142 | CTGGCTTTGCTGTTC[A/G]TGGGTACACCAACTT | 146845 |
| rs758311596 | snp | C/T | 3.32176e-05 | 0.00407526 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585996 | AGTGAAAACGACTCA[C/T]TGTCAATTTATCTAG | 146845 |
| rs758363267 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9597849 | AGAGAAAGAGAGAGA[C/G]AAAGAGAGAGAGAAA | 146845 |
| rs758369113 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9597571 | GCACTTTGGGAGGCT[A/G]AAGCGGATGGATCAC | 146845 |
| rs758431365 | snp | C/T | 1.64822e-05 | 0.00287068 | missense, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641809 | ATGGCATGGATATCA[C/T]ACAGGAAGGGGTGCA | 146845 |
| rs758495776 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9609165 | CATTCCAAGAAATCT[A/G]TGTTGAACATTCACG | 146845 |
| rs758509397 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9611387 | TGAGACAGAGTCTCA[C/T]TCTGTCATCCAGGAT | 146845 |
| rs758570869 | snp | A/T | 1.67466e-05 | 0.00289362 | missense, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643179 | CCATTTTGCGATGGA[A/T]GTACCCATATACCTC | 146845 |
| rs758588142 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9589338 | AGTTCTTCTCTTACT[A/G]TATAGCAAGTCAACA | 146845 |
| rs758620784 | in-del | -/CA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9580688 | AGTGAGACCTGGTCT[-/CA]AAAAAAAAAAAAAAA | 146845 |
| rs758622429 | snp | A/T | 3.7379e-05 | 0.00432297 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586860 | AAACATAGTTACTTA[A/T]TTTCTTTATTTTTTT | 146845 |
| rs758623097 | in-del | -/GA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636244 | AGAAAGAAAGAAAGA[-/GA]AAGAAAGAGAAAGAA | 146845 |
| rs758642314 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9578087 | ACAGAGCGAGACTCC[A/G]TCTCAAAAAATAAAT | 146845 |
| rs758645765 | snp | A/G | 1.67542e-05 | 0.00289427 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9598273 | GGATCTTCCAAATAG[A/G]AAAATCTGGCCAACT | 146845 |
| rs758688485 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9629496 | TTCTTTCTTTCTTTC[C/T]TTTCTTTTCTTTCTT | 146845 |
| rs758725045 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9587218 | TCTTTTTTATGGCTG[C/T]GTAGTAGTCCATGAT | 146845 |
| rs758741653 | snp | A/G | 1.66596e-05 | 0.00288609 | missense, upstream-variant-2KB, utr-variant-5-prime | CFAP52, STX8 | GRCh38.p7 | 17:9576738 | CAAGTGGCGGAGCTG[A/G]AACTTGACGCCGTGA | 146845 |
| rs758810453 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9622925 | AAATAGAATATTTCA[A/G]TATGTACTTTGGAGA | 146845 |
| rs758822123 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9586109 | TTGACTTCTCTTTTA[A/C]CCCATTTTCATTCCG | 146845 |
| rs758862623 | snp | A/G | 1.75702e-05 | 0.00296392 | intron-variant | CFAP52 | GRCh38.p7 | 17:9608266 | GTAGAGACCCACTAA[A/G]CGGAGATTTGCTTAA | 146845 |
| rs758936347 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9615371 | AAGAGAGTGTATTGT[C/T]TTTTTTCAACTCTTT | 146845 |
| rs758940196 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9611170 | TTGCACAAGAACCTG[A/C]GTTGAATTCTTCATT | 146845 |
| rs759017509 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9586149 | GAGTGAAGGACTCTG[A/C]TGATTTTATACCCGA | 146845 |
| rs759032880 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9638154 | GTGAATTAAAGATAC[A/G]TCGATGATTAAAACA | 146845 |
| rs759113189 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9592074 | ATCATAAAATTGACC[C/T]GTGTTAAGGTGTACA | 146845 |
| rs759149835 | snp | C/T | 9.89022e-05 | 0.00703145 | stop-gained | CFAP52 | GRCh38.p7 | 17:9632932 | GCCCCAGAGACAGGC[C/T]GACTGATGTATGTCA | 146845 |
| rs759230803 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9632214 | TCCCGAGTAGCTAGG[A/G]CTAAATGGGCATGCC | 146845 |
| rs759265015 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9585507 | CCCCGTCTCTACTAA[A/G]AATACAAAAAAAAAT | 146845 |
| rs759294731 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9599857 | AGCGATTCTCCTACC[G/T]CAGCCTCCCGAGTAG | 146845 |
| rs759350930 | snp | G/T | | | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642695 | TTGACTACAAAGCAG[G/T]TATCAAACTAGACAC | 146845 |
| rs759375500 | snp | C/T | 3.45006e-05 | 0.00415321 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586844 | CGGAAGGTAATGAAC[C/T]AAACATAGTTACTTA | 146845 |
| rs759402753 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9590685 | AGAGACTAGGTCTTG[C/T]GGGGAAAATGGCCCC | 146845 |
| rs759409222 | snp | A/G | 1.65059e-05 | 0.00287275 | missense | CFAP52 | GRCh38.p7 | 17:9638697 | CAGATCATCACCAGC[A/G]GAACAGACAGAAAGG | 146845 |
| rs759490636 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9592384 | TGAGGCAGGAGAATC[A/G]CTTGAACCCAGGAGG | 146845 |
| rs759502082 | snp | C/T | 1.64781e-05 | 0.00287033 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9612420 | CAGCTTCACGGATTT[C/T]AAAGAGACGCTCATA | 146845 |
| rs759504335 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9602901 | ATATGTTTGTTGGCC[A/G]CATAAATATCTTCTT | 146845 |
| rs759545507 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9630676 | ACCTCGTGATCCGCC[C/T]GCCTCGGTCTCCCAA | 146845 |
| rs759555147 | snp | C/G | 1.67624e-05 | 0.00289498 | intron-variant | CFAP52 | GRCh38.p7 | 17:9594173 | TGACTTTTTTTTTTT[C/G]GTCCCTCTTATTTTG | 146845 |
| rs759559976 | snp | C/T | 1.71032e-05 | 0.00292426 | intron-variant | CFAP52 | GRCh38.p7 | 17:9628661 | TGCATCTCTTGATGG[C/T]TTCCTTGCAGTGGCA | 146845 |
| rs759566278 | snp | A/G | 1.65616e-05 | 0.00287759 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641847 | ACAGGTTAGTCCTGG[A/G]ATAGGAAAAAGCCAA | 146845 |
| rs759632687 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9624703 | GACTCTGCCTTTTTT[C/T]TGAGTCATATTTTCC | 146845 |
| rs759672221 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9585154 | TTACGAGAATTGGCC[A/G]TAGGACTTGCTGGAC | 146845 |
| rs759717013 | snp | A/C/T | 3.36741e-05 | 0.00410319 | missense | CFAP52 | GRCh38.p7 | 17:9598239 | TTTTACATAGTGGGA[A/C/T]AATTCGAGTATGGGA | 146845 |
| rs759720203 | in-del | AATGCAGTAT/TCAAATATACAATGCAGTA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9584600 | CTCTTTTAGCAGATT[AATGCAGTAT/TCAAATATACAATGCAGTA]TTTTTTTTTAATTTA | 146845 |
| rs759787464 | snp | C/T | 3.32618e-05 | 0.00407797 | intron-variant | CFAP52 | GRCh38.p7 | 17:9594351 | TCGGAGTTTTCAGAA[C/T]TCATAAATTGCTATA | 146845 |
| rs759986321 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9635759 | AATTTCCAGGAAGAA[A/C]TGAATGTTAGAAGTT | 146845 |
| rs759988424 | snp | C/T | 3.29538e-05 | 0.00405904 | intron-variant, missense | CFAP52 | GRCh38.p7 | 17:9585907 | GGCAACAACGTCTCC[C/T]GCTTGGCCATCTCCA | 146845 |
| rs759994008 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9583531 | TGAGATCTTTATGAA[A/G]AAAATGGAAAATGCT | 146845 |
| rs760009668 | snp | A/G | 1.6486e-05 | 0.00287102 | synonymous-codon, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641750 | GGAAGTATTTGATGG[A/G]ACAGTAATCAGAGAA | 146845 |
| rs760096529 | in-del | -/C | 1.64776e-05 | 0.00287028 | frameshift-variant | CFAP52 | GRCh38.p7 | 17:9600084 | GGATGATGATGATAG[-/C]TTTTTCTACCTTGGC | 146845 |
| rs760109531 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636952 | CAGGAGGCTGAGGCA[G/T]GAGAATCGCTTGAAC | 146845 |
| rs760112887 | snp | A/G | 4.95184e-05 | 0.00497562 | intron-variant, synonymous-codon | CFAP52 | GRCh38.p7 | 17:9585957 | CTCCGGACAAGTCAC[A/G]TTCATGGGGTTCAAG | 146845 |
| rs760122542 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9594669 | CCCACCTGCTCTTGA[C/T]TGGGGTCTCATGATC | 146845 |
| rs760128408 | snp | G/T | 1.67186e-05 | 0.0028912 | missense | CFAP52 | GRCh38.p7 | 17:9633029 | GTGGCGGTGGGGAAG[G/T]GGAGGTATTGAAAGC | 146845 |
| rs760164540 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9598559 | TTGAGGTCATGAGTT[A/C]GAGACCAGCCTGGCC | 146845 |
| rs760165533 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9619988 | TTCAACATAGTGTTG[A/G]AAGTTCTGGCCAGGG | 146845 |
| rs760223918 | snp | A/G | 1.78899e-05 | 0.00299076 | intron-variant | CFAP52 | GRCh38.p7 | 17:9608072 | CATTCTTTAGTGGTG[A/G]TTTGTGAGATTTTTG | 146845 |
| rs760245054 | snp | C/T | 1.64817e-05 | 0.00287064 | intron-variant | CFAP52 | GRCh38.p7 | 17:9635395 | AGATCCTGTGCTCTG[C/T]GGCTTTCAGGTGAGG | 146845 |
| rs760332494 | in-del | -/A | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9611189 | AATTCTTCATTGTCT[-/A]AAACTAAACTAGTTA | 146845 |
| rs760354423 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9632016 | GTCCTCAAGTGATCC[A/G]CCTGCCTTGGCCTCC | 146845 |
| rs760375921 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9591743 | AATGAGCCAGGCACG[A/G]TGGTGTGTGCCTGTA | 146845 |
| rs760403031 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9597478 | ACATCATGATGTACA[A/C]CATAAATATATATTA | 146845 |
| rs760499389 | snp | A/G | 1.64792e-05 | 0.00287042 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9612429 | GGATTTCAAAGAGAC[A/G]CTCATAGCGACTTGT | 146845 |
| rs760512293 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631222 | TTTCTGTCCTCCTTT[A/G]CCTTCTTACCTGGAG | 146845 |
| rs760520489 | snp | C/G | 2.01181e-05 | 0.00317154 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575750 | GAAGCCCGGCCTCCC[C/G]GAAGGTCCCTCCACG | 146845 |
| rs760551631 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9602526 | CTATCCAGTCTATCA[C/T]TGATGGACATTTGGG | 146845 |
| rs760552565 | snp | G/T | 1.66308e-05 | 0.00288359 | intron-variant | CFAP52 | GRCh38.p7 | 17:9612512 | ACAAGAATGTGGAGA[G/T]TTGATGCAGTGTGCC | 146845 |
| rs760554493 | snp | G/T | 3.31581e-05 | 0.00407161 | intron-variant | CFAP52 | GRCh38.p7 | 17:9594189 | GTCCCTCTTATTTTG[G/T]CAGTGTGGTGGTGTG | 146845 |
| rs760570480 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9590512 | CAGCGAAAGAAAAGA[A/G]TTCCAACATCCTTCG | 146845 |
| rs760613607 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9630214 | CTTGCTTCTCTTCTC[A/G]CCCAGTATACTTTCC | 146845 |
| rs760630676 | snp | A/G | 1.65345e-05 | 0.00287524 | intron-variant | CFAP52 | GRCh38.p7 | 17:9628852 | AAGATCTGGCTTGGG[A/G]CTCTAGCTGCGGTTT | 146845 |
| rs760704752 | snp | G/T | 1.67234e-05 | 0.00289161 | intron-variant | CFAP52 | GRCh38.p7 | 17:9594370 | TAAATTGCTATATTT[G/T]CTTGCACAGAAAACA | 146845 |
| rs760723032 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9614842 | GACCTTGCCAAACTT[A/C]CCCTGGTGGCAAAAT | 146845 |
| rs760742300 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9594530 | CTGTGATTGCTGCTG[A/C]AAAGATTTTGCTTAC | 146845 |
| rs760755904 | snp | G/T | 1.68213e-05 | 0.00290006 | missense | CFAP52 | GRCh38.p7 | 17:9598245 | ATAGTGGGACAATTC[G/T]AGTATGGGAATTGGA | 146845 |
| rs760768674 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9634789 | GGAATACCATACTAA[C/T]TAAACAACTTCCCTT | 146845 |
| rs760811138 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9622629 | TTGGTCCCTGCTTAC[A/C]TGAAAATATGTTTGT | 146845 |
| rs760909924 | snp | G/T | 1.65436e-05 | 0.00287602 | intron-variant, splice-donor-variant | CFAP52 | GRCh38.p7 | 17:9585973 | TTCATGGGGTTCAAG[G/T]TGAATACAGTGAAAA | 146845 |
| rs760916169 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9582244 | ATTGTTTTCCAAAAC[G/T]ATTAGACCGATTTAC | 146845 |
| rs760943645 | snp | C/G/T | 0.000441666 | 0.0148548 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584285 | ACATGGAAGCAGTAG[C/G/T]GTTACCTTGGCAGAT | 146845 |
| rs760971007 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9633445 | CCTGACCTCAGATGA[A/T]CCACCTGCCTTGGCC | 146845 |
| rs760999645 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9629851 | CGCCTCGGCCTCCCA[A/G]AGTGATGGGATTACA | 146845 |
| rs761008098 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9608424 | TGAATCAAACCAAAG[G/T]AGTCCACTATTACCC | 146845 |
| rs761053990 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9599336 | TTCATTCTCCATGGA[C/T]TGATTCCTCTTGTTT | 146845 |
| rs761065382 | snp | A/G | 0.00028138 | 0.0118579 | missense, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643059 | AAGTTTGGGATTATA[A/G]TGAGGGTGAAGTGAC | 146845 |
| rs761143814 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9595479 | TAAAGCAACTGACCA[C/T]GGGCTGTGGCGACAC | 146845 |
| rs761146293 | snp | A/T | 1.64808e-05 | 0.00287057 | missense | CFAP52 | GRCh38.p7 | 17:9628767 | GGATCACCGTGCCCA[A/T]CATGACCTGCCACGG | 146845 |
| rs761196271 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9630023 | GAACACGGCTCAGGA[C/T]AGAAATCTTGGAGTC | 146845 |
| rs761197790 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9627459 | GAGTAAGCCAAGATC[A/G]GACCATTGCACTCCA | 146845 |
| rs761248950 | snp | C/T | | | upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576531 | CCATCTCTCTTCCAG[C/T]CCCCATACCCCTTCA | 146845 |
| rs761264835 | snp | C/T | 7.07314e-05 | 0.00594648 | intron-variant | CFAP52 | GRCh38.p7 | 17:9608086 | GATTTGTGAGATTTT[C/T]GTGCTTTTTCTTAAC | 146845 |
| rs761266784 | snp | A/C/G | 3.29523e-05 | 0.00405898 | missense | CFAP52 | GRCh38.p7 | 17:9635507 | AAGAGGAACAACGAG[A/C/G]AGTGTGTCACCGCCA | 146845 |
| rs761276680 | snp | C/T | | | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575252 | AGAAAGTGCAAAATG[C/T]CTTATAAACAAGTGC | 146845 |
| rs761277371 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9608633 | ATTGTGTTAATCATG[C/T]ATTTGAATACAATTT | 146845 |
| rs761321931 | snp | C/T | 1.65446e-05 | 0.00287612 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9608187 | AGCCGGACTGCTGGT[C/T]TTCTGTAAAAGCCCT | 146845 |
| rs761339518 | in-del | -/C | 1.64727e-05 | 0.00286986 | frameshift-variant | CFAP52 | GRCh38.p7 | 17:9635551 | TTGTATCATTTGGGA[-/C]CTTGTGTAGGTACCT | 146845 |
| rs761359822 | snp | A/G/T | 3.39272e-05 | 0.00411858 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586680 | CCCTATGATCTGACG[A/G/T]TGTGTTCTTGCCCCC | 146845 |
| rs761392759 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9586361 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTAGCC | 146845 |
| rs761414458 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9634048 | CCAGACGTTTTGACC[A/C]TTATTTTTAAATGAT | 146845 |
| rs761476823 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9629126 | AAGGACAGGTCCCCC[A/T]TGTGAGGACCCTTTT | 146845 |
| rs761504102 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9614499 | TTACTTAGTCTGATA[A/T]TAAGATTACCACATC | 146845 |
| rs761523039 | in-del | -/AA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631028 | GAAAGAAAGAAAGAA[-/AA]AGAGAGAGAGAGAGA | 146845 |
| rs761529529 | snp | C/T | 3.31719e-05 | 0.00407245 | intron-variant | CFAP52 | GRCh38.p7 | 17:9594337 | GTATGTGTCTGCGTT[C/T]GGAGTTTTCAGAACT | 146845 |
| rs761546633 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9577027 | TAAAAGGGACCAAAT[A/G]CCTCTTCCCCAGGCG | 146845 |
| rs761560030 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9587378 | ATATTCCTTTGAGTA[G/T]GTAGCCAGTAATGGG | 146845 |
| rs761568024 | snp | G/T | 1.65154e-05 | 0.00287358 | missense | CFAP52 | GRCh38.p7 | 17:9586803 | CCAAATGATTTGTAC[G/T]TGGTATCACTAGGAG | 146845 |
| rs761589218 | snp | A/G | 0.000184568 | 0.00960469 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641880 | CTGGCTTATTTAGAC[A/G]AGGACATGGAAGGAA | 146845 |
| rs761656094 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9583083 | TCTTTGATCTACCTG[A/G]AAGATATTGTTTGTG | 146845 |
| rs761659701 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9637987 | GTGGGTCTTGGGAGG[A/G]ACTTCTTACCATATG | 146845 |
| rs761708038 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9640515 | GTTTTCTGTTCCTGC[A/G]TTAGTTTGCTGAGGA | 146845 |
| rs761710255 | snp | A/G | 1.64776e-05 | 0.00287028 | missense | CFAP52 | GRCh38.p7 | 17:9635409 | GTGGCTTTCAGGTGA[A/G]GGTATGGCAGATAGG | 146845 |
| rs761714877 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9602309 | GCCCCGGTGTGTGAT[C/G]TTCCCCTCCCTGTGT | 146845 |
| rs761762667 | snp | A/G | 1.71319e-05 | 0.00292672 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598382 | GCACACGTTCCTGTT[A/G]GCAGTGCTGACCAAG | 146845 |
| rs761836671 | snp | C/T | 1.66635e-05 | 0.00288643 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | CFAP52, STX8 | GRCh38.p7 | 17:9576704 | CCCAAGGATGGATAA[C/T]AAAATTTCGCCGGAG | 146845 |
| rs761864975 | snp | A/G | 8.2464e-05 | 0.00642069 | missense | CFAP52 | GRCh38.p7 | 17:9638617 | TTTCCAGGCGTCTCA[A/G]GAGGAATCAGATGAT | 146845 |
| rs761894645 | snp | A/G | 1.64732e-05 | 0.0028699 | intron-variant, missense | CFAP52 | GRCh38.p7 | 17:9585797 | CCACTGGTCTCAAAT[A/G]CCATCCTGACCAGGA | 146845 |
| rs761903826 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB, intron-variant | CFAP52, USP43 | GRCh38.p7 | 17:9643907 | GAAGGGTGATGAAAT[A/G]GACCTTGTGTCCTTG | 146845 |
| rs761943639 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9613548 | TTTGAAGCGGAGTCT[C/T]GCTCTGTCACCCAGG | 146845 |
| rs762005540 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9581805 | CTTGGCAGCCAATTG[A/G]GAGATGTAACATAAT | 146845 |
| rs762064702 | snp | C/T | 0.0002653 | 0.0115143 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638718 | GACAGAAAGGTGAGT[C/T]CTCCCAGTGAGAGAT | 146845 |
| rs762140907 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9627258 | CTCACACCTGTAATC[C/T]CAGCACTTTGGGAGG | 146845 |
| rs762206085 | snp | A/G | 3.29989e-05 | 0.00406182 | missense | CFAP52 | GRCh38.p7 | 17:9632909 | ACGACGGTAAAATCC[A/G]AGCCTTCGCCCCAGA | 146845 |
| rs762284410 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9626528 | AGCCACTGCTCCTGA[C/T]CTGGAAAGTTCTTCG | 146845 |
| rs762307224 | snp | A/G | 3.31263e-05 | 0.00406965 | intron-variant | CFAP52 | GRCh38.p7 | 17:9628863 | TGGGGCTCTAGCTGC[A/G]GTTTTGATTCTTGTC | 146845 |
| rs762325050 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9605859 | TGTCCAAACCCAGAG[A/G]GTATGCAATGCCAAG | 146845 |
| rs762332370 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9586051 | CCACTTCAAGTTGTT[A/T]GTTCTATGTGGCAAT | 146845 |
| rs762360430 | snp | C/T | 1.67784e-05 | 0.00289636 | missense | CFAP52 | GRCh38.p7 | 17:9598263 | TATGGGAATTGGATC[C/T]TCCAAATAGAAAAAT | 146845 |
| rs762407977 | snp | C/G | 0.000134233 | 0.00819136 | intron-variant, missense | CFAP52 | GRCh38.p7 | 17:9586699 | GTTCTTGCCCCCAGG[C/G]AGACATCATTTTGTG | 146845 |
| rs762432421 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9627529 | AAATAAATGAATAAA[G/T]AAATAAATATTGTCT | 146845 |
| rs762478148 | snp | C/T | 1.65135e-05 | 0.00287341 | missense, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643149 | AATATATTGTTAGTG[C/T]AAGTGCCGATGGAGC | 146845 |
| rs762482958 | snp | C/T | 0.000115374 | 0.0075943 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9612327 | GATTCAGTTACAAGG[C/T]GGCATCACTTCTATC | 146845 |
| rs762568901 | in-del | -/AG | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636206 | GAAAGAAAGAAAGAA[-/AG]AAAGAAAGAAAGAAA | 146845 |
| rs762606736 | snp | A/G | 1.64909e-05 | 0.00287144 | missense, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643085 | GTGACTCACGTTGGG[A/G]TGGGACACAGTGGCA | 146845 |
| rs762620788 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9613502 | TTGTTTTTGGGGGGT[G/T]TTTGTTTGTTTGTTT | 146845 |
| rs762627357 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9586161 | CTGATGATTTTATAC[C/G]CGAGGTTGCAGCTTG | 146845 |
| rs762675491 | snp | A/C | 0.000461077 | 0.0151765 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584234 | ACCAACTCAAGCAAA[A/C]CAATAATTACATTCA | 146845 |
| rs762718772 | snp | C/T | 3.2956e-05 | 0.00405918 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9635518 | CGAGGAGTGTGTCAC[C/T]GCCAGCACCGATGGG | 146845 |
| rs762745416 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9633226 | TACTTATTTTGAAAT[A/G]GAGTCTCACTCTGTC | 146845 |
| rs762809080 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9581503 | CTATTACAGTTTAAA[A/G]TGTACATATGTTTGA | 146845 |
| rs762871417 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9580571 | ATGCATGCCTGTAGT[A/C]CCAGCTATTCGAGAG | 146845 |
| rs762886610 | snp | G/T | 1.66899e-05 | 0.00288871 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638734 | CTCCCAGTGAGAGAT[G/T]AGATCTTTCCAGCGC | 146845 |
| rs762897421 | snp | A/G | 1.6473e-05 | 0.00286988 | missense | CFAP52 | GRCh38.p7 | 17:9600103 | TTCTACCTTGGCACC[A/G]CGACTGGAGATATTC | 146845 |
| rs762901987 | in-del | -/CTTT | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9629478 | TCTTTCTTTCCCTTT[-/CTTT]CTTTCTTTCTTTCTT | 146845 |
| rs762960984 | in-del | -/AGAA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636252 | AAGAAAGAAAGAAAG[-/AGAA]AGAAAAATAACTAAT | 146845 |
| rs763013883 | snp | A/G | 1.64789e-05 | 0.0028704 | missense | CFAP52 | GRCh38.p7 | 17:9612433 | TTCAAAGAGACGCTC[A/G]TAGCGACTTGTCACT | 146845 |
| rs763026370 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9603830 | TCCCAGAACTTGAAG[G/T]ATAATTTTTAAAAAA | 146845 |
| rs763157395 | snp | C/T | 4.9476e-05 | 0.00497348 | missense, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641743 | CTTACTGGGAAGTAT[C/T]TGATGGGACAGTAAT | 146845 |
| rs763207562 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9626249 | GTTCTTCTTTTTTGA[A/G]ATGGAGTTTTGTTCT | 146845 |
| rs763218147 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9615984 | TTAAATATAGTTTTT[C/T]GGGGGGAGGAGCCAA | 146845 |
| rs763219383 | snp | A/T | 1.78707e-05 | 0.00298915 | intron-variant | CFAP52 | GRCh38.p7 | 17:9628621 | GGTGTCAAATATGCA[A/T]CTGGGAAACTGCATC | 146845 |
| rs763410156 | snp | C/G | 1.65168e-05 | 0.00287369 | missense | CFAP52 | GRCh38.p7 | 17:9632995 | ATCGCCACCACCAGT[C/G]ACTGTAAAAGGGTCA | 146845 |
| rs763470822 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9598139 | TAACGAAGCCTCAAA[A/C]ATGTTTAGATCTCTT | 146845 |
| rs763470934 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9585386 | TTATTTTTAAAGTGT[G/T]GGCCGGGCGCGGTGG | 146845 |
| rs763507137 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9620338 | CTACAAACCACTGCT[C/T]AAGGAAATAAAAGAG | 146845 |
| rs763510080 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9635992 | AGCCTGGCCAACATG[A/G]TGAAACCCCTTCTCT | 146845 |
| rs763538730 | snp | G/T | 3.29495e-05 | 0.00405877 | missense | CFAP52 | GRCh38.p7 | 17:9600135 | AAAAATGAACCCCAG[G/T]ACTAAACTGCTGACA | 146845 |
| rs763555959 | snp | G/T | 1.64806e-05 | 0.00287054 | intron-variant, missense | CFAP52 | GRCh38.p7 | 17:9585919 | TCCTGCTTGGCCATC[G/T]CCAGGTCTGGAGAGT | 146845 |
| rs763582624 | snp | A/G | 1.64808e-05 | 0.00287057 | intron-variant | CFAP52 | GRCh38.p7 | 17:9635397 | ATCCTGTGCTCTGTG[A/G]CTTTCAGGTGAGGGT | 146845 |
| rs763646782 | in-del | -/A | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9585168 | CGTAGGACTTGCTGG[-/A]CCAGCATCAGCATCA | 146845 |
| rs763702622 | snp | A/G | 1.77461e-05 | 0.00297871 | intron-variant | CFAP52 | GRCh38.p7 | 17:9608081 | GTGGTGATTTGTGAG[A/G]TTTTTGTGCTTTTTC | 146845 |
| rs763797482 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9627719 | GTTTTTATTTTATTT[A/C]ATTTTATTTTTAGAG | 146845 |
| rs763842835 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9610148 | ACAATCAGGAGAGGA[A/G]AGAAATAACATCCAA | 146845 |
| rs763958777 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9600511 | GCCTCTCAAAGTGCT[A/G]GGATTACAGGTGTGA | 146845 |
| rs763980338 | snp | C/T | 1.65853e-05 | 0.00287964 | intron-variant | CFAP52 | GRCh38.p7 | 17:9594190 | TCCCTCTTATTTTGG[C/T]AGTGTGGTGGTGTGG | 146845 |
| rs764002056 | snp | C/T | 6.04881e-05 | 0.00549913 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575756 | CGGCCTCCCCGAAGG[C/T]CCCTCCACGCACCGC | 146845 |
| rs764032293 | snp | C/T | 1.69378e-05 | 0.00291009 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633044 | GGGAGGTATTGAAAG[C/T]AGAAATTTGAAAAAA | 146845 |
| rs764033621 | snp | C/T | 1.6477e-05 | 0.00287024 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9594262 | CGGCCTCAATGTTGG[C/T]AATGCCACCAATGTG | 146845 |
| rs764064459 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9592534 | TCCATCCCTCCTCCT[C/T]CAAGCCCCAGGCAAC | 146845 |
| rs764065289 | in-del | -/TGT | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9607058 | TGTTTTAAAATCAAA[-/TGT]TGTGGCTGAGTGTGG | 146845 |
| rs764091622 | snp | A/G | 1.66485e-05 | 0.00288513 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | CFAP52, STX8 | GRCh38.p7 | 17:9576725 | TTCGCCGGAGGCCCA[A/G]GTGGCGGAGCTGGAA | 146845 |
| rs764099666 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9632433 | ATCAAGAAGATGACA[C/T]AATTTTTAAAAGGCC | 146845 |
| rs764138380 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9613540 | TGTTTGTTTTTGAAG[A/C]GGAGTCTTGCTCTGT | 146845 |
| rs764157498 | snp | A/G | 0.00020145 | 0.0100342 | missense | CFAP52 | GRCh38.p7 | 17:9598259 | CGAGTATGGGAATTG[A/G]ATCTTCCAAATAGAA | 146845 |
| rs764174400 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9598867 | TTGTTTTGCTGGAAT[C/G]TAGGCTGTCATCAAA | 146845 |
| rs764186245 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9633279 | GCTCAATCTTGGCTC[G/T]TTACAACCTCTGCCT | 146845 |
| rs764278898 | in-del | -/A/AA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636199 | AAGAAAGAAAGAAAG[-/A/AA]AAAGAAAGAAAGAAA | 146845 |
| rs764331106 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9626340 | GTTCAAGTGATTCTC[C/T]TTCCTCAGCCTCCCA | 146845 |
| rs764363818 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642911 | AAGTAAAAGTGTTAT[C/T]ATAAAGACAGATACA | 146845 |
| rs764406343 | snp | C/T | 1.64808e-05 | 0.00287057 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9628768 | GATCACCGTGCCCAA[C/T]ATGACCTGCCACGGC | 146845 |
| rs764423806 | snp | A/G | 3.29979e-05 | 0.00406175 | missense | CFAP52 | GRCh38.p7 | 17:9638611 | ATCTACTTTCCAGGC[A/G]TCTCAGGAGGAATCA | 146845 |
| rs764569895 | in-del | -/AA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631030 | AAGAAAGAAAGAAAG[-/AA]AGAGAGAGAGAGAGA | 146845 |
| rs764573491 | in-del | -/GGGGTCAGG | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9616196 | ACCTGGGAAGCGCAA[-/GGGGTCAGG]GAGTTCCCTTTCCCA | 146845 |
| rs764581655 | snp | C/G | | | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9574724 | TTTTTAGTAGAGACG[C/G]GGTTTCTCCATGTTG | 146845 |
| rs764605349 | snp | G/T | 5.16711e-05 | 0.00508261 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598183 | GGGATGAAGTGATTA[G/T]TAAATGGGTGTCCAT | 146845 |
| rs764647577 | snp | G/T | | | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575082 | GTTCAATAACAATAC[G/T]TTCCTTGGGATCAAA | 146845 |
| rs764668378 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9639224 | CACCTGAGGTCAGGA[A/G]TTCGAGACCAGCCTA | 146845 |
| rs764723109 | snp | C/T | 0.00011608 | 0.0076175 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585989 | TGAATACAGTGAAAA[C/T]GACTCATTGTCAATT | 146845 |
| rs764725291 | snp | A/G | 1.65562e-05 | 0.00287712 | missense | CFAP52 | GRCh38.p7 | 17:9608192 | GACTGCTGGTCTTCT[A/G]TAAAAGCCCTGGCTA | 146845 |
| rs764761966 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9627465 | GCCAAGATCGGACCA[C/T]TGCACTCCAGCCCAG | 146845 |
| rs764790949 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9586151 | GTGAAGGACTCTGAT[G/T]ATTTTATACCCGAGG | 146845 |
| rs764932913 | snp | A/G | 1.68454e-05 | 0.00290214 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641886 | TATTTAGACGAGGAC[A/G]TGGAAGGAACTCCCA | 146845 |
| rs764934553 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9638157 | AATTAAAGATACATC[A/G]ATGATTAAAACATAA | 146845 |
| rs764947992 | snp | A/G | 4.94385e-05 | 0.0049716 | missense | CFAP52 | GRCh38.p7 | 17:9628781 | AACATGACCTGCCAC[A/G]GCATCGACTTCATGA | 146845 |
| rs764962783 | in-del | -/TTACAGGC | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9613791 | CCCAAGGTGTTGGGA[-/TTACAGGC]GTGAGCCACTGCACC | 146845 |
| rs764983917 | snp | A/G | 4.94956e-05 | 0.00497447 | missense, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643079 | GGTGAAGTGACTCAC[A/G]TTGGGGTGGGACACA | 146845 |
| rs764994440 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9580554 | AATAGCCAGGCATGG[C/T]GATGCATGCCTGTAG | 146845 |
| rs765017068 | in-del | -/A | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9607591 | AACAATAAGAAGTCT[-/A]TTGTGCTTTCTTGGG | 146845 |
| rs765061731 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9611928 | CATAGCATCCTTTGA[C/T]GTAAAGCATCTTCCC | 146845 |
| rs765131270 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9584356 | ATGAAAGGTCCCAGG[C/T]TCTTCAGAGCACCTG | 146845 |
| rs765147380 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9598665 | ACTTGGGAGGTTGAG[A/G]CAGGAGAATTGCTTG | 146845 |
| rs765199360 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9600310 | ACAGTGACGTGATCT[G/T]GGCTCACTGCAACTT | 146845 |
| rs765294174 | snp | G/T | 1.64732e-05 | 0.0028699 | intron-variant, missense | CFAP52 | GRCh38.p7 | 17:9585805 | CTCAAATGCCATCCT[G/T]ACCAGGAGCATATGA | 146845 |
| rs765313459 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9590730 | TCTGGCAAAACTGTT[A/C]ATCTCTGCTGTAATT | 146845 |
| rs765323357 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9610560 | TTTGTTTTGAGATGG[A/T]GTCTCGCTCTGTTGC | 146845 |
| rs765338549 | snp | A/G | 1.66585e-05 | 0.00288599 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638729 | GAGTCCTCCCAGTGA[A/G]AGATGAGATCTTTCC | 146845 |
| rs765338836 | snp | A/G | 9.89087e-05 | 0.00703168 | missense | CFAP52 | GRCh38.p7 | 17:9638628 | CTCAGGAGGAATCAG[A/G]TGATACTAGCCAACA | 146845 |
| rs765358792 | snp | A/G | | | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575696 | CCCCTCATCCCGAAA[A/G]GCCACCAGCGGCAAT | 146845 |
| rs765465858 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9615276 | TTGTGTAATATTCTG[C/T]TAGGTTGGTGCAAAA | 146845 |
| rs765507258 | snp | A/G | 1.65641e-05 | 0.00287781 | intron-variant | CFAP52 | GRCh38.p7 | 17:9628864 | GGGGCTCTAGCTGCG[A/G]TTTTGATTCTTGTCA | 146845 |
| rs765517839 | snp | C/T | 1.6476e-05 | 0.00287014 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9612369 | AGAAGGACACCAGTT[C/T]CTCGTAGGAACAGAA | 146845 |
| rs765570854 | snp | C/T | 1.64789e-05 | 0.0028704 | missense | CFAP52 | GRCh38.p7 | 17:9612430 | GATTTCAAAGAGACG[C/T]TCATAGCGACTTGTC | 146845 |
| rs765637945 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9585227 | TCAACCCCTTCTCAG[A/G]CCTGAAATCAGAATC | 146845 |
| rs765701771 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9594696 | GATCTGATAGTTTGC[A/G]AATGAATTCTGCCAG | 146845 |
| rs765720763 | snp | A/G | | | intron-variant, splice-acceptor-variant | CFAP52 | GRCh38.p7 | 17:9586697 | GTGTTCTTGCCCCCA[A/G]GCAGACATCATTTTG | 146845 |
| rs765779784 | snp | A/G | 1.64838e-05 | 0.00287083 | missense, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643098 | GGGTGGGACACAGTG[A/G]CAACATCACACGCAT | 146845 |
| rs765912584 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9598605 | TGTCTCTACTAAAAA[C/T]ACACAAGTAGCCAGG | 146845 |
| rs765999786 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9597575 | TTTGGGAGGCTGAAG[C/T]GGATGGATCACGAGG | 146845 |
| rs766012051 | snp | A/G | 1.65209e-05 | 0.00287405 | missense, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643152 | ATATTGTTAGTGTAA[A/G]TGCCGATGGAGCCAT | 146845 |
| rs766093848 | snp | C/T | 1.70417e-05 | 0.002919 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632843 | ACTGTGGAGAGAGGG[C/T]GCATATACTGATCCT | 146845 |
| rs766135724 | snp | A/T | 0.000144749 | 0.0085061 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584239 | CTCAAGCAAAACAAT[A/T]ATTACATTCAAGCAT | 146845 |
| rs766153158 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9638072 | GCTTTCCGAGGGTTG[C/T]GCATGATATGGTACG | 146845 |
| rs766179265 | snp | A/G | 8.23906e-05 | 0.00641783 | missense | CFAP52 | GRCh38.p7 | 17:9635519 | GAGGAGTGTGTCACC[A/G]CCAGCACCGATGGGA | 146845 |
| rs766189489 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9577983 | TGTAATCCCAGCTAC[A/T]TGAGAGGCTGAGGGA | 146845 |
| rs766234347 | snp | A/T | 1.68043e-05 | 0.0028986 | intron-variant | CFAP52 | GRCh38.p7 | 17:9608222 | ACAAACCCATCAAGT[A/T]AGTTCCGGGTCTCAC | 146845 |
| rs766245608 | snp | A/C | 1.64803e-05 | 0.00287052 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9612333 | GTTACAAGGCGGCAT[A/C]ACTTCTATCACACTT | 146845 |
| rs766311234 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9610161 | GAAAGAAATAACATC[C/T]AAGTATTGTCGATAA | 146845 |
| rs766313738 | in-del | -/CTT | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9586080 | TGTGCTTTATTCTTC[-/CTT]CTTCTTCTTCTTTTT | 146845 |
| rs766324859 | snp | A/G | 1.65674e-05 | 0.00287809 | missense | CFAP52 | GRCh38.p7 | 17:9586722 | ATTTTGTGGGATTAT[A/G]AGAACAGAGAGCTGC | 146845 |
| rs766347200 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9588677 | TTTCACCCCATTCAG[G/T]GTGATAATTTGCTGT | 146845 |
| rs766382154 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9601747 | TCAAAGGATAATTTT[A/T]TATAACAAATGCTGC | 146845 |
| rs766413263 | snp | C/T | 3.57596e-05 | 0.0042283 | intron-variant | CFAP52 | GRCh38.p7 | 17:9628623 | TGTCAAATATGCATC[C/T]GGGAAACTGCATCTT | 146845 |
| rs766472420 | snp | C/T | 1.64789e-05 | 0.0028704 | missense | CFAP52 | GRCh38.p7 | 17:9612434 | TCAAAGAGACGCTCA[C/T]AGCGACTTGTCACTT | 146845 |
| rs766482167 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9629274 | CACCTCTAAAGACTT[C/T]AGCATGTATCTCTAA | 146845 |
| rs766522329 | snp | A/G | 1.65217e-05 | 0.00287412 | stop-gained | CFAP52 | GRCh38.p7 | 17:9594204 | GCAGTGTGGTGGTGT[A/G]GAGCATAGCCAAGAG | 146845 |
| rs766542481 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9630078 | ATGCCCACATCCACA[C/T]CCCCTGCTGATGCTC | 146845 |
| rs766593871 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9634896 | TTCACTCCAGGATAA[C/T]ACACAGGTATTTGGA | 146845 |
| rs766609885 | in-del | -/TTAAT | 0.000821961 | 0.020256 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598341 | GTATTGGAGTAAGTA[-/TTAAT]TTAAGTATTAAGTAA | 146845 |
| rs766648979 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9593880 | CGAGGCAGGAGAATC[A/G]CTTGAATCCAGGAGG | 146845 |
| rs766651607 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9596337 | AACTCCTGAGCTCAG[G/T]CAATCCACCTGCCTC | 146845 |
| rs766670022 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9583201 | AAAAAATTTTTAGTA[A/G]GAATAGATCACCCTA | 146845 |
| rs766683990 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9615039 | CTTCGCCTTTTAATA[A/T]GTAAGGGTAACTTTC | 146845 |
| rs766777954 | in-del | -/CTCACCCGGGA | 0.000103536 | 0.00719424 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575776 | CCACGCACCGCCGCC[-/CTCACCCGGGA]CTCACCAGGGGTCCG | 146845 |
| rs766780153 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9594619 | AGAAACAATTTGCAC[A/G]ATTGCACAGATTCAC | 146845 |
| rs766807437 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9610323 | TATGATGAAGATAAA[C/T]TCAAAGTAATTATCA | 146845 |
| rs766843037 | snp | C/G | 3.32635e-05 | 0.00407807 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600023 | TGATATTACAGGCGT[C/G]AGCCACCGAGGCTGG | 146845 |
| rs766848223 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9607157 | TCGAGACCAGCCTGG[C/G]CAACATGGCGAAACC | 146845 |
| rs766865404 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9582267 | CGATTTACTCTCCCA[C/T]CAAGCATTTTATGAG | 146845 |
| rs766869580 | in-del | -/A | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9622544 | GACCCTGTTTCTATT[-/A]AAAAAAAAAAGAAGA | 146845 |
| rs766883955 | in-del | -/GAA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636181 | TCTGTCTCAAAAAAA[-/GAA]AGAAAGAAAGAAAGA | 146845 |
| rs766916666 | in-del | -/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9599659 | TTTGTAAGTCTTCAT[-/G]GGGTGCCAGAGGAAC | 146845 |
| rs766919743 | snp | A/G | 1.64844e-05 | 0.00287087 | missense | CFAP52 | GRCh38.p7 | 17:9632933 | CCCCAGAGACAGGCC[A/G]ACTGATGTATGTCAT | 146845 |
| rs766939707 | snp | C/T | 1.64762e-05 | 0.00287016 | intron-variant, missense | CFAP52 | GRCh38.p7 | 17:9585902 | GTCATGGCAACAACG[C/T]CTCCTGCTTGGCCAT | 146845 |
| rs767006074 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9595254 | TGTTCAGTAGAACTA[C/T]TTTTTTCAACCCATC | 146845 |
| rs767012938 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9586460 | CCCAGCTACTCGGGA[C/G]GCTGAGACAGGGAGA | 146845 |
| rs767024203 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9597116 | TTCTACTGTCTCATG[C/T]GTTAGGCTTTTTTAC | 146845 |
| rs767028110 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9588703 | GCTGTGGGTTTGTCA[C/T]ATAGGGTCTTTATCA | 146845 |
| rs767125884 | in-del | -/AAAT | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9578095 | AGACTCCGTCTCAAA[-/AAAT]AAATAAATAAATAAA | 146845 |
| rs767149548 | in-del | -/AAA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9622004 | AACTTAGAGTATAAT[-/AAA]AAAAAAATAAATAAA | 146845 |
| rs767171945 | snp | A/C | 0.000132602 | 0.00814146 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600039 | AGCCACCGAGGCTGG[A/C]CAAGATTTCTTTTTC | 146845 |
| rs767219781 | snp | A/T | 1.6473e-05 | 0.00286988 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9600156 | ACTGCTGACAGATGT[A/T]GGGCCTGCGAAGGAC | 146845 |
| rs767225381 | snp | C/G | | | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9577813 | CTCTGCAACTGAGGC[C/G]GGGGGCAGTGGCTCA | 146845 |
| rs767269118 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9638021 | ACAAGGGTTGAGCCT[G/T]CCAGCTTTTGGGACA | 146845 |
| rs767282833 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9627912 | ATTTTTATTTTTTGG[G/T]GAGGCAGGGTCTCAC | 146845 |
| rs767325986 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9587591 | GTGGTTATCTCATTG[C/T]GGTTTTACTTTGCAT | 146845 |
| rs767383747 | snp | C/T | 1.66913e-05 | 0.00288883 | intron-variant | CFAP52 | GRCh38.p7 | 17:9594175 | ACTTTTTTTTTTTGG[C/T]CCCTCTTATTTTGGC | 146845 |
| rs767391328 | snp | A/C/G | 0.000103488 | 0.00719267 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586845 | GGAAGGTAATGAACT[A/C/G]AACATAGTTACTTAT | 146845 |
| rs767415440 | snp | A/G | 1.64757e-05 | 0.00287012 | missense | CFAP52 | GRCh38.p7 | 17:9612350 | CTTCTATCACACTTC[A/G]AGGAGAAGGACACCA | 146845 |
| rs767426799 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9578011 | GGAGGAGAATCACTT[G/T]AACTTGGGAGGCAGA | 146845 |
| rs767449476 | snp | A/G | 1.6543e-05 | 0.00287597 | missense, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643158 | TTAGTGTAAGTGCCG[A/G]TGGAGCCATTTTGCG | 146845 |
| rs767468275 | snp | A/T | 3.29565e-05 | 0.00405921 | missense | CFAP52 | GRCh38.p7 | 17:9612423 | CTTCACGGATTTCAA[A/T]GAGACGCTCATAGCG | 146845 |
| rs767512491 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9600440 | TACAGACAGGGTTTC[A/G]TCATGTTGGCTAGGC | 146845 |
| rs767576439 | snp | C/T | 1.64838e-05 | 0.00287083 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9628759 | GCTGCTGCGGATCAC[C/T]GTGCCCAACATGACC | 146845 |
| rs767604734 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9614730 | GTGGATGCTATTCTG[A/T]GCATTAAAGGATGTT | 146845 |
| rs767626504 | snp | A/G | 4.94311e-05 | 0.00497123 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9594277 | CAATGCCACCAATGT[A/G]ATCTTCTCCAGGTGC | 146845 |
| rs767632079 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9639930 | GGCAGTCAAGTTCCA[A/G]CTACTTCTGTGGGTG | 146845 |
| rs767782726 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9633356 | ATTACAGGCGCACAC[A/C]GTCATGCCCAGCTAA | 146845 |
| rs767841634 | in-del | -/AAAGAAA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636196 | AAGAAAGAAAGAAAG[-/AAAGAAA]GAAAGAAAGAAAGAA | 146845 |
| rs767855879 | in-del | -/AAAA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9578113 | AAATAAATAAATAAA[-/AAAA]CAAACAAACATACAT | 146845 |
| rs767892841 | in-del | -/AGAAAGAG | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636246 | GAAAGAAAGAAAGAA[-/AGAAAGAG]AAAGAAAAATAACTA | 146845 |
| rs767894196 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9593822 | ATACAAGAATTACCC[A/G]GACATGGTGGTGTGC | 146845 |
| rs767922630 | snp | C/T | 1.64779e-05 | 0.00287031 | intron-variant, missense | CFAP52 | GRCh38.p7 | 17:9585911 | ACAACGTCTCCTGCT[C/T]GGCCATCTCCAGGTC | 146845 |
| rs767960979 | snp | C/T | | | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9574976 | CAATTATAAACTATA[C/T]TAGAAATAACAACAT | 146845 |
| rs767965356 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9595100 | TTCACCACATTGGCC[A/G]GGTTGGTCTCCAACT | 146845 |
| rs767997507 | in-del | -/A/AAA | 3.30225e-05 | 0.0040633 | frameshift-variant, cds-indel | CFAP52 | GRCh38.p7 | 17:9632901 | GCATGGAACGACGGT[-/A/AAA]AAAATCCGAGCCTTC | 146845 |
| rs768008484 | in-del | -/TTGGCG | 1.72151e-05 | 0.00293381 | cds-indel, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643222 | AGATGTCTCTGAGCC[-/TTGGCG]TTGCACGCAGTCCTG | 146845 |
| rs768049366 | snp | A/G | 3.30344e-05 | 0.004064 | intron-variant, missense | CFAP52 | GRCh38.p7 | 17:9585963 | ACAAGTCACATTCAT[A/G]GGGTTCAAGGTGAAT | 146845 |
| rs768055665 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9629255 | TATAGGCAGCGTGAT[A/G]TTCCACCTCTAAAGA | 146845 |
| rs768084713 | snp | A/C | 1.6631e-05 | 0.00288362 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641859 | TGGGATAGGAAAAAG[A/C]CAAGCCTGGCTTATT | 146845 |
| rs768098168 | in-del | -/TTT | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9629492 | TTCTTTCTTTCTTTC[-/TTT]CTTTTCTTTTCTTTC | 146845 |
| rs768138371 | in-del | -/GAG | | | cds-indel | CFAP52 | GRCh38.p7 | 17:9612350 | CTTCTATCACACTTC[-/GAG]GAGAAGGACACCAGT | 146845 |
| rs768196533 | in-del | -/TGGCACCACGAC | 1.64738e-05 | 0.00286995 | cds-indel | CFAP52 | GRCh38.p7 | 17:9600096 | TAGCTTTTTCTACCT[-/TGGCACCACGAC]TGGAGATATTCTAAA | 146845 |
| rs768255997 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9588386 | TGCCCAGAGAGACAA[A/T]GAGTTAAGTTGCTGA | 146845 |
| rs768286409 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9601177 | ACAAAAAACCAAACA[C/T]CACATTTTCTTACTC | 146845 |
| rs768299972 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9582916 | TGCTGGGATTACAGG[C/T]ATGAGCCACCCAGCC | 146845 |
| rs768311432 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9602298 | ACCCCTGACAGGCCC[C/T]GGTGTGTGATGTTCC | 146845 |
| rs768322615 | snp | A/C/T | 6.72262e-05 | 0.00579734 | intron-variant | CFAP52 | GRCh38.p7 | 17:9635607 | TGCAAAATCCAATCA[A/C/T]GCCAACAGTTTATTG | 146845 |
| rs768341853 | snp | G/T | | | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9577685 | TGCTTTATACATTTC[G/T]GATATCAGATATCTT | 146845 |
| rs768343939 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9589956 | TTCTCCTTCTTGGCC[C/G]GGAGGTGCTCTTCAC | 146845 |
| rs768349856 | snp | A/G | 1.67891e-05 | 0.00289729 | missense, upstream-variant-2KB, utr-variant-5-prime | CFAP52, STX8 | GRCh38.p7 | 17:9576762 | GCCGTGATCGGCTTC[A/G]ATGGTGAGGCCTCCA | 146845 |
| rs768387591 | snp | C/G | 1.64857e-05 | 0.00287099 | missense | CFAP52 | GRCh38.p7 | 17:9628745 | TCATCCAACAGGGAG[C/G]TGCTGCGGATCACCG | 146845 |
| rs768433333 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9635570 | GTGTAGGTACCTGTG[A/T]TGGGGAGGATGCAGT | 146845 |
| rs768477260 | in-del | -/AA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9588384 | CGTGCCCAGAGAGAC[-/AA]AGAGTTAAGTTGCTG | 146845 |
| rs768509604 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9622424 | CTGGACATGTTGGTG[G/T]CACTGCCTCTAGTCC | 146845 |
| rs768614574 | snp | A/G | 3.30344e-05 | 0.004064 | missense | CFAP52 | GRCh38.p7 | 17:9632899 | CCAGCATGGAACGAC[A/G]GTAAAATCCGAGCCT | 146845 |
| rs768716014 | in-del | -/GAT | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9622573 | GAAGAAGAAGAAGAA[-/GAT]GATGATGATGATGAG | 146845 |
| rs768716890 | snp | C/G | | | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575643 | TGTGGCGGGATGTGG[C/G]TGAGCCCCCTCAGTA | 146845 |
| rs768754989 | snp | G/T | | | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642774 | ATAGAGAAAAGACTG[G/T]AAGGAACTAAGCCAA | 146845 |
| rs768783628 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9593746 | CAGATGTGAGCCATC[A/G]CTCCCAGCCAACATT | 146845 |
| rs768820074 | in-del | -/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9607175 | CATGGCGAAACCCCA[-/T]TCTCTACTGAAAATA | 146845 |
| rs768830852 | snp | C/T | 1.64923e-05 | 0.00287156 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9632970 | TGCTCACAGGATCGG[C/T]GTCACCGCCATCGCC | 146845 |
| rs768841227 | snp | A/C/G | 5.09276e-05 | 0.00504595 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586679 | TCCCTATGATCTGAC[A/C/G]GTGTGTTCTTGCCCC | 146845 |
| rs768842024 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9606809 | AGCCTTCATCCTGTT[C/G]TCCTGCTGAGGCACT | 146845 |
| rs768901707 | snp | C/G/T | 0.000197672 | 0.00993978 | intron-variant, synonymous-codon | CFAP52 | GRCh38.p7 | 17:9585789 | ACATGTGCCCACTGG[C/G/T]CTCAAATGCCATCCT | 146845 |
| rs768950617 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9585119 | GCTGCTCACACTCCA[G/T]GCATTCGTGCTTTTT | 146845 |
| rs768997804 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9599494 | GAGGATGCCTATTAA[C/T]ATCAGAACCAGATAG | 146845 |
| rs769000395 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9638048 | GACATCCCCACGTGA[A/C]AGGCTCGTGCTTTCC | 146845 |
| rs769013396 | snp | C/T | 0.000124481 | 0.00788829 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586873 | TATTTTCTTTATTTT[C/T]TTTAACTTTTATTTC | 146845 |
| rs769016321 | snp | C/G | 1.64814e-05 | 0.00287061 | intron-variant, missense | CFAP52 | GRCh38.p7 | 17:9585923 | GCTTGGCCATCTCCA[C/G]GTCTGGAGAGTACAT | 146845 |
| rs769038172 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9627197 | ACCATTGTCTTTTCC[C/T]TTTTGAAAATTTTAA | 146845 |
| rs769123006 | snp | G/T | 1.65064e-05 | 0.00287279 | missense | CFAP52 | GRCh38.p7 | 17:9586797 | TTTTCTCCAAATGAT[G/T]TGTACTTGGTATCAC | 146845 |
| rs769163108 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9626315 | GCTCACTGCAACCTC[C/T]GCCTCCTGGGTTCAA | 146845 |
| rs769230477 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9628606 | TGTGAAACACATTTT[G/T]GTGTCAAATATGCAT | 146845 |
| rs769232501 | in-del | -/AAAGAA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631023 | AAGAAAGAAAGAAAG[-/AAAGAA]AGAGAGAGAGAGAGA | 146845 |
| rs769315942 | in-del | -/TC | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9602774 | ACATCCTCCCCAGCA[-/TC]TGTTGTTTCCTGACT | 146845 |
| rs769322582 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9640343 | TCATCCCATCACCTC[A/G]GTATTAAGCCCTGCA | 146845 |
| rs769347632 | snp | A/C | 1.66203e-05 | 0.00288268 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638584 | GAGAAAGTCGACTTT[A/C]ACAGCTTTTGAATCT | 146845 |
| rs769377252 | snp | C/T | 1.65963e-05 | 0.0028806 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585727 | GTAGAAAATTCCTGG[C/T]CACTTCTGCACCTGA | 146845 |
| rs769414152 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9601197 | TTTTCTTACTCATAG[G/T]TGGGAATTGAACAAT | 146845 |
| rs769417106 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9594865 | ATTCACTAATTAGAA[C/G]CTTGTTTAAATTAGC | 146845 |
| rs769452748 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9593548 | GCGACCTCCACCTCC[C/T]GGATTCAAGCGATTC | 146845 |
| rs769465711 | snp | C/T | 4.94287e-05 | 0.00497111 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9612396 | AGAAGAATCGCACAT[C/T]TATCGTGTCAGCTTC | 146845 |
| rs769469875 | snp | C/T | 1.6543e-05 | 0.00287597 | missense | CFAP52 | GRCh38.p7 | 17:9586813 | TGTACTTGGTATCAC[C/T]AGGAGGCCCAGATGA | 146845 |
| rs769499969 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631992 | TGACCAGGCTGGTCT[C/T]CACCTCCTGTCCTCA | 146845 |
| rs769532217 | snp | A/G | 1.6867e-05 | 0.002904 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598230 | GTTTTTTTTTTTTAC[A/G]TAGTGGGACAATTCG | 146845 |
| rs769533731 | in-del | -/T | 1.68792e-05 | 0.00290505 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638562 | AGTGAATAAATTTCC[-/T]AGGGAAGAGAAAGTC | 146845 |
| rs769573926 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9606689 | TTATTTAGAAATCAC[A/T]CATATGTAGCTTCGA | 146845 |
| rs769607076 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9614435 | TGCTGGGATTACAGG[C/T]GTGAGCCACCACGCC | 146845 |
| rs769642521 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9581431 | CTAATGAGGAAAGAT[G/T]TCAAAGATATATTAA | 146845 |
| rs769673846 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB, intron-variant | CFAP52, USP43 | GRCh38.p7 | 17:9643617 | CTCAGATTTAAATCC[A/G]GATCTTGGGCAGGCT | 146845 |
| rs769686571 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9612147 | TTTGCTGTTCGTGGG[G/T]ACACCAACTTGTGAG | 146845 |
| rs769698584 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9600105 | CTACCTTGGCACCAC[A/G]ACTGGAGATATTCTA | 146845 |
| rs769736611 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9613386 | TTTCATGAAGTTGGT[C/T]AGTTTTTGCTCTGAA | 146845 |
| rs769739399 | in-del | -/TTTT | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9613504 | TTTTTGGGGGGTTTT[-/TTTT]TGTTTGTTTGTTTGT | 146845 |
| rs769822678 | snp | G/T | 1.76921e-05 | 0.00297418 | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576816 | GGAATTCGGAGGACG[G/T]GTAGTGCAAACAGGA | 146845 |
| rs769825446 | snp | A/G | 1.64757e-05 | 0.00287012 | intron-variant, missense | CFAP52 | GRCh38.p7 | 17:9585896 | TACAGGGTCATGGCA[A/G]CAACGTCTCCTGCTT | 146845 |
| rs769927424 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9605312 | TTTATAGGAAAAGAA[A/G]GAAACTGAGATGCAC | 146845 |
| rs769952159 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9639680 | GAAAGGACTGAGAAA[A/G]GAGATAGAACTGGTG | 146845 |
| rs770066348 | snp | C/T | 1.65507e-05 | 0.00287664 | missense, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641725 | TTCCTGAATTCCAGA[C/T]TGCTTACTGGGAAGT | 146845 |
| rs770126670 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9611106 | GTCATTAACTGTTCT[A/G]TGTCCCACCAATAAA | 146845 |
| rs770178005 | snp | C/T | 9.04343e-05 | 0.00672376 | upstream-variant-2KB, stop-gained, nc-transcript-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575792 | TCACCCGGGACTCAC[C/T]AGGGGTCCGGTGCCA | 146845 |
| rs770267271 | snp | C/G | 1.65021e-05 | 0.00287241 | missense, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643146 | ATCAATATATTGTTA[C/G]TGTAAGTGCCGATGG | 146845 |
| rs770317001 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9581242 | GAATGGCGTGAACCC[A/G]GAAGTGCTGGTTGCA | 146845 |
| rs770318141 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636905 | CAAAAAGTAGCTGGG[C/T]GTGGTGGCGCGTGCC | 146845 |
| rs770318304 | snp | A/G | 3.46909e-05 | 0.00416464 | utr-variant-3-prime, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643227 | TCTCTGAGCCTTGGC[A/G]TTGCACGCAGTCCTG | 146845 |
| rs770324536 | snp | C/T | 1.6495e-05 | 0.0028718 | missense | CFAP52 | GRCh38.p7 | 17:9632912 | ACGGTAAAATCCGAG[C/T]CTTCGCCCCAGAGAC | 146845 |
| rs770335445 | in-del | -/AGAGAGAGACAG | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9610020 | GAGAGAGACAGAGAC[-/AGAGAGAGACAG]AGAGAGAGAGAAGCT | 146845 |
| rs770407483 | snp | A/G | 1.64779e-05 | 0.00287031 | missense | CFAP52 | GRCh38.p7 | 17:9612416 | GTGTCAGCTTCACGG[A/G]TTTCAAAGAGACGCT | 146845 |
| rs770451010 | snp | A/G | 3.2993e-05 | 0.00406145 | missense | CFAP52 | GRCh38.p7 | 17:9632977 | AGGATCGGCGTCACC[A/G]CCATCGCCACCACCA | 146845 |
| rs770482221 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9594161 | CTGTTTTCTCTTTGA[C/T]TTTTTTTTTTTGGTC | 146845 |
| rs770507362 | snp | C/T | 1.75841e-05 | 0.00296509 | utr-variant-3-prime, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643235 | CCTTGGCGTTGCACG[C/T]AGTCCTGTTGAAGAC | 146845 |
| rs770538356 | in-del | -/TT | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9625749 | ATCTACTTTTAGAGG[-/TT]TTTGGTGTCATTAAG | 146845 |
| rs770569173 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9579925 | ACTTGACACTTGTAG[A/G]TATTGCATTTTGGCA | 146845 |
| rs770574506 | snp | A/C | | | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642674 | GAATTAAGTTTCACA[A/C]GTACATTGACTACAA | 146845 |
| rs770582163 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9614298 | GTAGCTGGGACTACA[A/G]GCATGTGCCACCGCG | 146845 |
| rs770653745 | snp | A/C | 3.36587e-05 | 0.00410222 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598349 | GTAAGTATTAATTTA[A/C]GTATTAAGTAACAAT | 146845 |
| rs770668824 | snp | A/G | 1.65233e-05 | 0.00287426 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638600 | ACAGCTTTTGAATCT[A/G]CTTTCCAGGCGTCTC | 146845 |
| rs770695329 | snp | A/G | 1.65116e-05 | 0.00287324 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585754 | CTGATTATTATTACT[A/G]TGAATCTCTCTCTTT | 146845 |
| rs770702936 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9605106 | GCTATTTACCCAAAG[A/G]AGCTGAAAACTTATG | 146845 |
| rs770719369 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9592295 | TAGTGAAACCCTGTC[G/T]CTACTAAAAATGCAA | 146845 |
| rs770818084 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9626132 | CTTAACCTCTCAGAC[A/C]CTAAACTAAGAACAA | 146845 |
| rs770852429 | in-del | -/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9629499 | TTCTTTCTTTCTTTT[-/C]CTTTTCTTTCTTTCT | 146845 |
| rs770889866 | in-del | -/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9587204 | TCTCATGATCTCATT[-/C]TTTTTTATGGCTGCG | 146845 |
| rs770895321 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9603702 | AGCACAATATTGATA[C/G]CTAATGTAGATGACG | 146845 |
| rs770941718 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9609460 | AGCTCTTTGGGAGGT[C/T]GAGGCAAGTGGATCG | 146845 |
| rs771101957 | in-del | -/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9611288 | TAAAGGGAAGAGGGA[-/G]AAATCTGAAATGTAG | 146845 |
| rs771106495 | snp | C/T | 3.36553e-05 | 0.00410201 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586023 | CTAGAGGTGCCTCCC[C/T]AGAAGAACTGCCCCA | 146845 |
| rs771125247 | in-del | -/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9633594 | ACTAGAGTTAAGGAA[-/T]TCATGCGGGTGTTTT | 146845 |
| rs771135978 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9611881 | GGGTATTTAGGTTGT[C/T]TCCAACCTTTTACTC | 146845 |
| rs771167165 | snp | C/T | 1.72677e-05 | 0.00293829 | synonymous-codon, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643024 | TTTATCTTTTTCAGG[C/T]GGAAATGACCATCTG | 146845 |
| rs771216537 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9609443 | CTCACGCCTGCAATC[A/C]CAGCTCTTTGGGAGG | 146845 |
| rs771283670 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9629834 | ACCTCAGGCAATCCA[C/G]CCGCCTCGGCCTCCC | 146845 |
| rs771302579 | snp | A/G | | | upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576570 | AATGCTAATGAACTC[A/G]AACTCGGCAGGCTGG | 146845 |
| rs771305232 | snp | C/G | | | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9577524 | AGATTTTAGGAGAAG[C/G]AAAACTTTTCAAAAA | 146845 |
| rs771413878 | snp | A/G/T | 6.6185e-05 | 0.00575228 | synonymous-codon, missense | CFAP52 | GRCh38.p7 | 17:9633006 | CAGTGACTGTAAAAG[A/G/T]GTCATCAGTGGCGGT | 146845 |
| rs771417584 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9588366 | GACACAGCTCAGCCC[A/G]CTCGTGCCCAGAGAG | 146845 |
| rs771469131 | snp | A/G | 3.29913e-05 | 0.00406135 | intron-variant | CFAP52 | GRCh38.p7 | 17:9635368 | CCCTTCAGAAGTCCC[A/G]AGTGTGGATCAAGAT | 146845 |
| rs771478037 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631727 | ATAAAGGAGTTTGGA[C/T]TGGATTTTAATTCTA | 146845 |
| rs771479704 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9628882 | TTGATTCTTGTCACT[C/G]TCCTCCCATACTAGT | 146845 |
| rs771479940 | in-del | -/AAAGAA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636240 | AAGAAAGAAAGAAAG[-/AAAGAA]AGAAAGAGAAAGAAA | 146845 |
| rs771541433 | snp | A/T | 8.25117e-05 | 0.00642254 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9594316 | GATGTTTATGACTGC[A/T]GGAAAGTATGTGTCT | 146845 |
| rs771593633 | snp | C/T | 3.29544e-05 | 0.00405908 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600208 | GACCATCGCCACTGC[C/T]CTGCCATTTTTCTCC | 146845 |
| rs771596812 | snp | C/G | 1.68459e-05 | 0.00290219 | utr-variant-5-prime, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576681 | GGAGAGCAAAGTAAT[C/G]AGAACCTCCCAAGGA | 146845 |
| rs771661731 | in-del | -/A | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9625189 | AGCAGTAGAATCCTT[-/A]AAAAAAAATCAATTA | 146845 |
| rs771723256 | in-del | -/T/TT/TTT | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9591030 | TAGTTTGCATGCATC[-/T/TT/TTT]TTTTTTTTTTTTTTT | 146845 |
| rs771769282 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9578880 | GGCCTTAGGTCCTGT[C/T]TATAATTTGATATCT | 146845 |
| rs771788923 | in-del | -/AAGAAAG | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636192 | AAAAAGAAAGAAAGA[-/AAGAAAG]AAGAAAGAAAGAAAG | 146845 |
| rs771800618 | snp | G/T | 1.64751e-05 | 0.00287007 | intron-variant, missense | CFAP52 | GRCh38.p7 | 17:9585886 | CAGAACTTCCTACAG[G/T]GTCATGGCAACAACG | 146845 |
| rs771858098 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9629992 | AGGAGCTCTGGGCTT[A/G]CCTTACATCTAGAGC | 146845 |
| rs771988198 | snp | A/G | 1.65277e-05 | 0.00287464 | missense | CFAP52 | GRCh38.p7 | 17:9638706 | ACCAGCGGAACAGAC[A/G]GAAAGGTGAGTCCTC | 146845 |
| rs771996883 | in-del | -/A | 1.65949e-05 | 0.00288048 | intron-variant | CFAP52 | GRCh38.p7 | 17:9612498 | GTAGAAGAGAAAAAC[-/A]AAGAATGTGGAGATT | 146845 |
| rs772024985 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641612 | CAGCCAGTATCATCC[C/T]GTGGTGTATTTTTGC | 146845 |
| rs772032994 | snp | C/T | 1.67435e-05 | 0.00289335 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641708 | TCCTGCTTAATGCTT[C/T]TTTCCTGAATTCCAG | 146845 |
| rs772078430 | in-del | -/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9627471 | ATCGGACCATTGCAC[-/T]CCAGCCCAGGCAACA | 146845 |
| rs772160639 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9635667 | GAAATCTTATTTAAG[G/T]CAACACAGTAAAGGG | 146845 |
| rs772186858 | snp | A/T | 1.65149e-05 | 0.00287353 | intron-variant | CFAP52 | GRCh38.p7 | 17:9628841 | GTCCACATGTCAAGA[A/T]CTGGCTTGGGGCTCT | 146845 |
| rs772215485 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9577334 | AGACCAGGACAGAAG[A/G]GGAAGGGGACGCCAG | 146845 |
| rs772270093 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9594451 | ACATCATAGTTTTTG[C/T]GATTTTGTACTCATT | 146845 |
| rs772282768 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9596701 | CTTACTCCTCCTCAT[C/G]GTTGTTGTGTGTGTG | 146845 |
| rs772414698 | snp | C/T | 1.64746e-05 | 0.00287002 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9635485 | ATCAGTGTCCTGCAT[C/T]AGGGTGAAGAGGAAC | 146845 |
| rs772461992 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9586647 | GGGTAGCTATCTCCT[C/G]AGATGCTTTTAATGC | 146845 |
| rs772482168 | snp | A/C | | | upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576432 | ACTCTACACAAGGGG[A/C]TGGAGGAATTAGTTC | 146845 |
| rs772510455 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9606928 | ATCACAAAATGTCTT[C/T]TGAGCCACAACAGGC | 146845 |
| rs772543322 | snp | A/G | 1.6516e-05 | 0.00287362 | missense | CFAP52 | GRCh38.p7 | 17:9608164 | GGGGGTTTGTTGGTG[A/G]GCTCTGGAGCCGGAC | 146845 |
| rs772592263 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9600935 | GTCCTGAATTAGGGA[A/G]TCAGAACCACATTTC | 146845 |
| rs772668146 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9614843 | ACCTTGCCAAACTTC[A/C]CCTGGTGGCAAAATT | 146845 |
| rs772674669 | snp | C/T | 1.64914e-05 | 0.00287149 | stop-gained | CFAP52 | GRCh38.p7 | 17:9612316 | CCCTAAAGGAAGATT[C/T]AGTTACAAGGCGGCA | 146845 |
| rs772711709 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9590311 | ATCCAGCCAGGGAAT[A/G]GACAGTCACAGGCTT | 146845 |
| rs772718872 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9579848 | GCTGGGATTACAGGC[A/G]TGAGCCACTGCGACT | 146845 |
| rs772739520 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9611389 | AGACAGAGTCTCACT[C/T]TGTCATCCAGGATGG | 146845 |
| rs772740645 | snp | C/T | 6.82198e-05 | 0.00583997 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586665 | ATGCTTTTAATGCCT[C/T]CCTATGATCTGACGG | 146845 |
| rs772742570 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9610093 | TAATACAGGTGAGGT[C/G]GGGGAGAGGAATGAT | 146845 |
| rs772801131 | snp | C/G | 3.32276e-05 | 0.00407586 | missense | CFAP52 | GRCh38.p7 | 17:9586824 | TCACTAGGAGGCCCA[C/G]ATGACGGAAGGTAAT | 146845 |
| rs772854469 | snp | A/C | 1.71361e-05 | 0.00292707 | intron-variant | CFAP52 | GRCh38.p7 | 17:9594146 | TCTTATTTTAAAAGC[A/C]TGTTTTCTCTTTGAC | 146845 |
| rs772986431 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9630138 | CCTCATTATCTTCCC[C/T]CTTATCCTAGCCACC | 146845 |
| rs772986705 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642529 | CTTGGGAGGCTGAGA[C/T]AGGAGAATTGCTTGA | 146845 |
| rs773014521 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9588545 | CTGCCTACAGCCCCC[A/G]AGTGTTCTTTCTGCT | 146845 |
| rs773034503 | snp | A/G | 3.37177e-05 | 0.00410582 | splice-acceptor-variant | CFAP52 | GRCh38.p7 | 17:9598233 | TTTTTTTTTTACATA[A/G]TGGGACAATTCGAGT | 146845 |
| rs773045810 | snp | C/T | 4.9516e-05 | 0.00497549 | synonymous-codon, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643147 | TCAATATATTGTTAG[C/T]GTAAGTGCCGATGGA | 146845 |
| rs773119476 | snp | G/T | 1.66499e-05 | 0.00288525 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | CFAP52, STX8 | GRCh38.p7 | 17:9576713 | GGATAACAAAATTTC[G/T]CCGGAGGCCCAAGTG | 146845 |
| rs773141472 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9602517 | ATTTTCTTTCTATCC[A/G]GTCTATCATTGATGG | 146845 |
| rs773159621 | snp | A/G | 0.000198511 | 0.00996073 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584219 | TTTAGTGAATAAACT[A/G]CCAACTCAAGCAAAA | 146845 |
| rs773204041 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9609152 | CACCAGCTGTCTTCA[C/T]TCCAAGAAATCTGTG | 146845 |
| rs773205741 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9635698 | ATGTTCATCAGAAGC[C/T]GTTCATGACGGTCCA | 146845 |
| rs773265594 | snp | A/T | 1.6489e-05 | 0.00287128 | intron-variant, missense | CFAP52 | GRCh38.p7 | 17:9585943 | GGAGAGTACATCGCC[A/T]CCGGACAAGTCACAT | 146845 |
| rs773367785 | snp | C/G | 1.67815e-05 | 0.00289663 | intron-variant | CFAP52 | GRCh38.p7 | 17:9612526 | ATTTGATGCAGTGTG[C/G]CAGGGCATTTAATTT | 146845 |
| rs773409022 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9606934 | AAATGTCTTTTGAGC[C/T]ACAACAGGCTAAATT | 146845 |
| rs773421407 | in-del | -/AAAT | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9604751 | CAAGACTCTGTCTCA[-/AAAT]AAATAAATAAATAAA | 146845 |
| rs773506070 | snp | C/T | | | upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576468 | AGTTAGTGCCATCCC[C/T]TAAATTTCCAGAGAA | 146845 |
| rs773525212 | snp | A/C | | | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575158 | CCTTGGGATTAACTG[A/C]TAAATAAATCACCCT | 146845 |
| rs773537959 | snp | A/G | 1.65116e-05 | 0.00287324 | synonymous-codon, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641834 | GGTGCACTTTGTCAC[A/G]GGTTAGTCCTGGGAT | 146845 |
| rs773562310 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9601169 | TTCCAAGAACAAAAA[A/G]CCAAACACCACATTT | 146845 |
| rs773606802 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9627340 | CATGGTGAAACCCCG[A/T]CTCTACTAAAAATAC | 146845 |
| rs773639295 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9594529 | TCTGTGATTGCTGCT[G/T]AAAAGATTTTGCTTA | 146845 |
| rs773650058 | snp | C/T | 9.99717e-05 | 0.00706936 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9586829 | AGGAGGCCCAGATGA[C/T]GGAAGGTAATGAACT | 146845 |
| rs773673795 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9595440 | CTAATTGACCGGCAC[A/G]AAAACCAGCCCTACC | 146845 |
| rs773709019 | snp | C/T | 0.000228493 | 0.0106862 | intron-variant | CFAP52 | GRCh38.p7 | 17:9594162 | TGTTTTCTCTTTGAC[C/T]TTTTTTTTTTGGTCC | 146845 |
| rs773773738 | snp | C/G | | | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575732 | GTGATTGCCTGCTCT[C/G]CGGAAGCCCGGCCTC | 146845 |
| rs773841851 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9602299 | CCCCTGACAGGCCCC[A/G]GTGTGTGATGTTCCC | 146845 |
| rs773855575 | in-del | -/AA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631024 | AGAAAGAAAGAAAGA[-/AA]GAAAGAGAGAGAGAG | 146845 |
| rs773874671 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9640490 | TGTAAGTGAGAACAT[G/T]TGGTGTTTGGTTTTC | 146845 |
| rs773968679 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9622486 | TTTGAGGCTACCATG[A/G]GCTACAATCACACCA | 146845 |
| rs773994928 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9586355 | GATCCCCTGAGGTCA[G/T]GAGTTCGAGACCAGC | 146845 |
| rs774068552 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9641491 | TCTGTCTTAATCCAG[A/G]TTTATCAGCACATCA | 146845 |
| rs774112899 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9587236 | AGTAGTCCATGATGT[A/G]TATGTACCACATTTT | 146845 |
| rs774174672 | in-del | -/AG | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9581535 | AGAGAGAGAGGGGAT[-/AG]AGAGAGAGGAGAGGG | 146845 |
| rs774176812 | snp | C/G | 1.64925e-05 | 0.00287158 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585764 | TTACTGTGAATCTCT[C/G]TCTTTTAGGACATGT | 146845 |
| rs774200783 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9588428 | GGGTAGAGCTGGCTG[C/T]GCAGCTGTATGTGGG | 146845 |
| rs774221667 | snp | C/T | 1.64784e-05 | 0.00287035 | missense | CFAP52 | GRCh38.p7 | 17:9612418 | GTCAGCTTCACGGAT[C/T]TCAAAGAGACGCTCA | 146845 |
| rs774257338 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9634580 | GGGTGACAGAGCGAC[A/G]TTTTGTCTCAAAAAA | 146845 |
| rs774282830 | snp | A/T | 1.64776e-05 | 0.00287028 | missense | CFAP52 | GRCh38.p7 | 17:9612340 | GGCGGCATCACTTCT[A/T]TCACACTTCGAGGAG | 146845 |
| rs774316028 | snp | C/T | 1.65097e-05 | 0.00287308 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638605 | TTTTGAATCTACTTT[C/T]CAGGCGTCTCAGGAG | 146845 |
| rs774326668 | in-del | -/ACAC | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9606385 | CCCTGTCTCCAAAAT[-/ACAC]ACACACACACACACA | 146845 |
| rs774449567 | snp | G/T | 1.65567e-05 | 0.00287716 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641846 | CACAGGTTAGTCCTG[G/T]GATAGGAAAAAGCCA | 146845 |
| rs774470421 | in-del | -/AA | | | frameshift-variant | CFAP52 | GRCh38.p7 | 17:9612421 | AGCTTCACGGATTTC[-/AA]AGAGACGCTCATAGC | 146845 |
| rs774494211 | snp | A/G | 1.64836e-05 | 0.0028708 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9628753 | CAGGGAGCTGCTGCG[A/G]ATCACCGTGCCCAAC | 146845 |
| rs774501117 | snp | C/T | 1.65976e-05 | 0.00288072 | intron-variant | CFAP52 | GRCh38.p7 | 17:9594343 | GTCTGCGTTCGGAGT[C/T]TTCAGAACTCATAAA | 146845 |
| rs774511959 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9593759 | TCGCTCCCAGCCAAC[A/G]TTCGAAACCATCCTG | 146845 |
| rs774546371 | snp | A/C | 1.64906e-05 | 0.00287142 | intron-variant | CFAP52 | GRCh38.p7 | 17:9635380 | CCCAAGTGTGGATCA[A/C]GATCCTGTGCTCTGT | 146845 |
| rs774556937 | snp | G/T | 3.41577e-05 | 0.00413251 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586655 | ATCTCCTCAGATGCT[G/T]TTAATGCCTCCCTAT | 146845 |
| rs774581813 | snp | C/T | | | downstream-variant-500B, upstream-variant-2KB, intron-variant | CFAP52, USP43 | GRCh38.p7 | 17:9643851 | TACAGAGATGCTTTA[C/T]TGGAGTTGGCCATTA | 146845 |
| rs774619043 | snp | A/G | 6.59957e-05 | 0.005744 | intron-variant | CFAP52 | GRCh38.p7 | 17:9628826 | ATCATTTCAGGTAAC[A/G]TCCACATGTCAAGAT | 146845 |
| rs774691883 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9605595 | CAGCTACTCGGGAGG[C/T]TGAGGCAGGAGAATT | 146845 |
| rs774709991 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9594984 | CAACCTCCACCTCCC[A/G]GGTTCAAGCAATTCT | 146845 |
| rs774736100 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9638055 | CCACGTGACAGGCTC[A/G]TGCTTTCCGAGGGTT | 146845 |
| rs774738034 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9638787 | GTGGTGGAGGGTGCG[C/G]GCTCTGGAGTCAAAC | 146845 |
| rs774779660 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9606837 | ACTTAGGAAGTTAGG[G/T]GTGAGGGGTGGAAGC | 146845 |
| rs774814549 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9626316 | CTCACTGCAACCTCC[A/G]CCTCCTGGGTTCAAG | 146845 |
| rs774822586 | snp | A/G | 0.000362343 | 0.0134551 | missense | CFAP52 | GRCh38.p7 | 17:9600152 | CTAAACTGCTGACAG[A/G]TGTTGGGCCTGCGAA | 146845 |
| rs774843109 | in-del | -/GT | 1.64806e-05 | 0.00287054 | frameshift-variant | CFAP52 | GRCh38.p7 | 17:9638653 | CAACACCTTATTCCA[-/GT]GTGTGTGTGCTATCA | 146845 |
| rs774844698 | snp | G/T | 0.000141113 | 0.00839862 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575818 | TGCCATCCTGCAGAC[G/T]CCGCCCGCCGCTCGG | 146845 |
| rs774884333 | snp | C/T | 1.64887e-05 | 0.00287125 | synonymous-codon, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641747 | CTGGGAAGTATTTGA[C/T]GGGACAGTAATCAGA | 146845 |
| rs774949333 | snp | C/T | 3.29516e-05 | 0.00405891 | intron-variant, missense | CFAP52 | GRCh38.p7 | 17:9585905 | ATGGCAACAACGTCT[C/T]CTGCTTGGCCATCTC | 146845 |
| rs774949419 | snp | A/C | 1.64789e-05 | 0.0028704 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600212 | ATCGCCACTGCCCTG[A/C]CATTTTTCTCCCTTC | 146845 |
| rs774972360 | in-del | -/T | 1.6646e-05 | 0.00288491 | intron-variant | CFAP52 | GRCh38.p7 | 17:9594180 | TTTTTTTGGTCCCTC[-/T]TTATTTTGGCAGTGT | 146845 |
| rs774998612 | snp | C/T | 3.29891e-05 | 0.00406122 | intron-variant, stop-gained | CFAP52 | GRCh38.p7 | 17:9585949 | TACATCGCCTCCGGA[C/T]AAGTCACATTCATGG | 146845 |
| rs775006460 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9628939 | CCTCCCACTGTCCAC[C/T]CCCTTCTTGCTTCTA | 146845 |
| rs775063335 | snp | G/T | 1.64743e-05 | 0.00287 | missense | CFAP52 | GRCh38.p7 | 17:9635488 | AGTGTCCTGCATTAG[G/T]GTGAAGAGGAACAAC | 146845 |
| rs775082235 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9586977 | ATCAACCAGGTGCTC[A/G]GCCTAGTACCCAGTA | 146845 |
| rs775112192 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9612172 | TGTGAGTAACTCCTG[A/C]CTTTTCAACTGTGTC | 146845 |
| rs775143983 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9639556 | CCTGCTCTCATGAAC[C/G]TTACTTCCCTAATTT | 146845 |
| rs775150640 | snp | C/T | 1.6486e-05 | 0.00287102 | intron-variant | CFAP52 | GRCh38.p7 | 17:9635390 | GATCAAGATCCTGTG[C/T]TCTGTGGCTTTCAGG | 146845 |
| rs775171372 | snp | A/G | 1.66991e-05 | 0.00288951 | utr-variant-5-prime, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576694 | ATCAGAACCTCCCAA[A/G]GATGGATAACAAAAT | 146845 |
| rs775173029 | in-del | -/AGAG | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636249 | GAAAGAAAGAAAGAA[-/AGAG]AGAGAAAGAAAAATA | 146845 |
| rs775197198 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9581439 | GAAAGATGTCAAAGA[C/T]ATATTAAGTATAAAA | 146845 |
| rs775259713 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9592498 | AATAAAAAGAAACCC[C/T]GTACCCATTAGCAAT | 146845 |
| rs775261804 | snp | C/T | 1.64732e-05 | 0.0028699 | missense | CFAP52 | GRCh38.p7 | 17:9600101 | TTTTCTACCTTGGCA[C/T]CACGACTGGAGATAT | 146845 |
| rs775278092 | snp | A/C | 3.29881e-05 | 0.00406115 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600233 | TTCTCCCTTCACTGG[A/C]AGCATGTACTTTTTT | 146845 |
| rs775318716 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9613418 | TTCCTCAGTACTTAG[C/T]TTAATTTATAATACT | 146845 |
| rs775348504 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9601198 | TTTCTTACTCATAGG[C/T]GGGAATTGAACAATG | 146845 |
| rs775365315 | in-del | -/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9614159 | CTTTTCTTTCTTTCT[-/T]TTTTTTTTTTTTTTT | 146845 |
| rs775386115 | snp | A/G | 1.66189e-05 | 0.00288256 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641717 | ATGCTTCTTTCCTGA[A/G]TTCCAGATTGCTTAC | 146845 |
| rs775398261 | snp | C/T | | | downstream-variant-500B, upstream-variant-2KB, intron-variant | CFAP52, USP43 | GRCh38.p7 | 17:9643723 | GAATTAAGTGACTAA[C/T]GTACTAAAGCATCGG | 146845 |
| rs775423603 | snp | A/C | | | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575487 | CCAGCCAGCTAGCTC[A/C]AAAACCAGGATGGGC | 146845 |
| rs775443400 | snp | A/T | 1.65935e-05 | 0.00288036 | intron-variant | CFAP52 | GRCh38.p7 | 17:9594186 | TTGGTCCCTCTTATT[A/T]TGGCAGTGTGGTGGT | 146845 |
| rs775458752 | snp | C/T | 1.64784e-05 | 0.00287035 | missense | CFAP52 | GRCh38.p7 | 17:9612428 | CGGATTTCAAAGAGA[C/T]GCTCATAGCGACTTG | 146845 |
| rs775463266 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9580559 | CCAGGCATGGCGATG[C/G]ATGCCTGTAGTCCCA | 146845 |
| rs775515100 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9633217 | ATAAATGTATACTTA[G/T]TTTGAAATGGAGTCT | 146845 |
| rs775516550 | snp | C/T | 1.65261e-05 | 0.0028745 | intron-variant | CFAP52 | GRCh38.p7 | 17:9628847 | ATGTCAAGATCTGGC[C/T]TGGGGCTCTAGCTGC | 146845 |
| rs775551983 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9593603 | TGGGACTACAGGTGT[G/T]TGCCACCACATCCAG | 146845 |
| rs775576964 | snp | C/T | 0.000114804 | 0.00757554 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584267 | CATACAAACTTTTCT[C/T]TAACATGGAAGCAGT | 146845 |
| rs775592517 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642762 | ACCAGTATACTTATA[A/G]AGAAAAGACTGGAAG | 146845 |
| rs775622521 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9586305 | GCGGTGGCTCATGCC[C/T]GTAATCCCAGCACTT | 146845 |
| rs775639416 | snp | C/T | 1.68267e-05 | 0.00290053 | stop-gained | CFAP52 | GRCh38.p7 | 17:9598244 | CATAGTGGGACAATT[C/T]GAGTATGGGAATTGG | 146845 |
| rs775698776 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9601976 | CAGTTTTCTTAGTCA[C/T]ATAATCATTTAATAT | 146845 |
| rs775700519 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9639730 | GGGAAAGCTCCTTCA[A/G]CTGGGGTGGTGGGTG | 146845 |
| rs775757885 | snp | C/T | 3.36825e-05 | 0.00410367 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598351 | AAGTATTAATTTAAG[C/T]ATTAAGTAACAATTA | 146845 |
| rs775783114 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9603775 | AACCACTATGGCACA[C/T]GTACACCTATGTAAC | 146845 |
| rs775839033 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9625042 | CTCAAGCTCTGACAC[C/T]TGAAGCCTGTGAGGT | 146845 |
| rs775840253 | in-del | -/A | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9635302 | CAGGGAATTAAAAAA[-/A]CACAAATCAAGCATA | 146845 |
| rs775844485 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9625942 | CCATAATGTTTCTGA[A/C]CTATGTGATGATACT | 146845 |
| rs775857432 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9626244 | AGAAAGTTCTTCTTT[C/T]TTGAGATGGAGTTTT | 146845 |
| rs775972101 | snp | G/T | 1.6522e-05 | 0.00287414 | intron-variant, missense | CFAP52 | GRCh38.p7 | 17:9585967 | GTCACATTCATGGGG[G/T]TCAAGGTGAATACAG | 146845 |
| rs775981739 | in-del | -/AAAGAAAGAAAGAAAGAAAG | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636180 | ACTCTGTCTCAAAAA[-/AAAGAAAGAAAGAAAGAAAG]AAAGAAAGAAAGAAA | 146845 |
| rs776033317 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636912 | TAGCTGGGCGTGGTG[G/T]CGCGTGCCTGTTATC | 146845 |
| rs776094587 | snp | A/G | 1.70388e-05 | 0.00291875 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586669 | TTTTAATGCCTCCCT[A/G]TGATCTGACGGTGTG | 146845 |
| rs776124001 | snp | C/T | 0.000118031 | 0.00768124 | synonymous-codon, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643036 | AGGTGGAAATGACCA[C/T]CTGGTCAAAGTTTGG | 146845 |
| rs776152213 | snp | A/G | 1.64757e-05 | 0.00287012 | missense | CFAP52 | GRCh38.p7 | 17:9635505 | TGAAGAGGAACAACG[A/G]GGAGTGTGTCACCGC | 146845 |
| rs776156310 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9591969 | CAAAAGGATCCAAAA[C/T]TCAAAAGCATGACTC | 146845 |
| rs776158744 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9599765 | TTTTTTCCTGAGACA[A/G]AGTTTTGCTCTTGTT | 146845 |
| rs776166856 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9638129 | TGACATCTTGCTACA[A/G]CTTTTATTTGTGAAT | 146845 |
| rs776242745 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9628566 | ACAGGTTTGAGCCAC[C/T]GCGCCCAGCCTTTTC | 146845 |
| rs776266650 | snp | A/T | 1.68165e-05 | 0.00289965 | missense, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576764 | CGTGATCGGCTTCAA[A/T]GGTGAGGCCTCCAGC | 146845 |
| rs776327748 | snp | C/T | | | downstream-variant-500B, utr-variant-5-prime, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643501 | CACAGACCTTCCTCA[C/T]GATCTGTGCACAGAC | 146845 |
| rs776337185 | snp | A/C | 1.6504e-05 | 0.00287258 | intron-variant | CFAP52 | GRCh38.p7 | 17:9612306 | TTGTGCTTCTCCCTA[A/C]AGGAAGATTCAGTTA | 146845 |
| rs776412886 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9633160 | CCAAATTGACATTTT[A/G]ATGAGATCTGAAAAT | 146845 |
| rs776460331 | snp | A/C/T | 3.29664e-05 | 0.00405984 | synonymous-codon, missense | CFAP52 | GRCh38.p7 | 17:9628751 | AACAGGGAGCTGCTG[A/C/T]GGATCACCGTGCCCA | 146845 |
| rs776538399 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9624382 | ATCTTTTTAAAATTA[C/T]GTAATCTCTATTAAA | 146845 |
| rs776539772 | snp | A/G | 3.29538e-05 | 0.00405904 | missense | CFAP52 | GRCh38.p7 | 17:9594264 | GCCTCAATGTTGGCA[A/G]TGCCACCAATGTGAT | 146845 |
| rs776599920 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9586243 | TGTTGCTGTCATGTT[C/T]GTAGAACCTGATCCG | 146845 |
| rs776601298 | snp | A/C | 1.64806e-05 | 0.00287054 | intron-variant | CFAP52 | GRCh38.p7 | 17:9635398 | TCCTGTGCTCTGTGG[A/C]TTTCAGGTGAGGGTA | 146845 |
| rs776618101 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9590627 | ACCCCCGGAGATTCT[C/T]GGAGCTAGGCCATTA | 146845 |
| rs776664378 | snp | G/T | 1.65693e-05 | 0.00287826 | intron-variant | CFAP52 | GRCh38.p7 | 17:9594334 | AAAGTATGTGTCTGC[G/T]TTCGGAGTTTTCAGA | 146845 |
| rs776716850 | snp | A/G | 0.000166731 | 0.00912894 | missense, upstream-variant-2KB, utr-variant-5-prime | CFAP52, STX8 | GRCh38.p7 | 17:9576700 | ACCTCCCAAGGATGG[A/G]TAACAAAATTTCGCC | 146845 |
| rs776720835 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9609464 | CTTTGGGAGGTCGAG[A/G]CAAGTGGATCGCTTG | 146845 |
| rs776814442 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9594631 | CACAATTGCACAGAT[A/T]CACCTACTGACTGAT | 146845 |
| rs776839422 | snp | C/T | 3.30316e-05 | 0.00406383 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9586802 | TCCAAATGATTTGTA[C/T]TTGGTATCACTAGGA | 146845 |
| rs776879597 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9596778 | TGTAGTGCAGTGGCA[C/T]GATCTCGGCTCACTG | 146845 |
| rs776897931 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636438 | CCATAGAATGACTAA[C/G]TTCAAACTAACTAGA | 146845 |
| rs776929151 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9609472 | GGTCGAGGCAAGTGG[A/C]TCGCTTGAGCCCAGG | 146845 |
| rs776935857 | snp | C/T | 8.28192e-05 | 0.00643449 | intron-variant | CFAP52 | GRCh38.p7 | 17:9628862 | TTGGGGCTCTAGCTG[C/T]GGTTTTGATTCTTGT | 146845 |
| rs776962700 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9583510 | ATAAATGTAATAAGA[A/G]ATGAGTGAGATCTTT | 146845 |
| rs776969514 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9585143 | GCTTTTTAGGATTAC[A/G]AGAATTGGCCGTAGG | 146845 |
| rs777042524 | snp | A/T | 1.65751e-05 | 0.00287876 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638717 | AGACAGAAAGGTGAG[A/T]CCTCCCAGTGAGAGA | 146845 |
| rs777046120 | snp | C/T | | | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9577579 | TTAAGAATGTGGATG[C/T]AGAACAATCACTGTC | 146845 |
| rs777114820 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9628908 | CTAGTCTCTACATGT[A/G]GATAACCTAGAACAG | 146845 |
| rs777156974 | snp | A/T | 4.95127e-05 | 0.00497533 | missense, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643077 | AGGGTGAAGTGACTC[A/T]CGTTGGGGTGGGACA | 146845 |
| rs777210226 | snp | C/G | 1.64958e-05 | 0.00287187 | missense, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643142 | GGAAATCAATATATT[C/G]TTAGTGTAAGTGCCG | 146845 |
| rs777244447 | snp | C/T | 1.71472e-05 | 0.00292802 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641679 | ATGTGCATGGATGAC[C/T]CTCCTGAGCTGAGTC | 146845 |
| rs777291573 | snp | G/T | 1.64808e-05 | 0.00287057 | missense | CFAP52 | GRCh38.p7 | 17:9612450 | AGCGACTTGTCACTT[G/T]GATGCTGTCGAGGAT | 146845 |
| rs777302720 | snp | A/G | 1.6483e-05 | 0.00287076 | missense | CFAP52 | GRCh38.p7 | 17:9638676 | TGCTATCACCCTGAG[A/G]AGTTCCAGATCATCA | 146845 |
| rs777330972 | snp | A/G | 1.64735e-05 | 0.00286993 | intron-variant, synonymous-codon | CFAP52 | GRCh38.p7 | 17:9585855 | AGTCCTCATTCAGGC[A/G]ATAAATACTAAAGAG | 146845 |
| rs777376498 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9626598 | CCATGAGTACACCTC[G/T]TTAAGAGCTTACTTC | 146845 |
| rs777378417 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9632860 | CATATACTGATCCTG[A/C]CTGCCTTTTGTTTCC | 146845 |
| rs777397593 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9628202 | AGAGGGCATTAAATA[C/G]CGTTTACACAAGATG | 146845 |
| rs777442880 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9582201 | GTCCTGGGGCATGTG[C/T]GCATTCAAGCATCAT | 146845 |
| rs777463971 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9606336 | TACAGTGAGCTGTGA[C/T]TGTGCCACTGCACTC | 146845 |
| rs777498797 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9625703 | CCCTTTCCAGTTGCA[A/C]TCTTAGAAGAGCAAA | 146845 |
| rs777521115 | snp | C/T | 1.67276e-05 | 0.00289197 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632874 | GCCTGCCTTTTGTTT[C/T]CCTTTCATGCCAGCA | 146845 |
| rs777531946 | snp | C/T | 1.67323e-05 | 0.00289239 | missense | CFAP52 | GRCh38.p7 | 17:9598317 | GACAGTTGAAAAGAA[C/T]AGTCATGAGTATTGG | 146845 |
| rs777540698 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9592062 | TACATTTCACATATC[A/C]TAAAATTGACCCGTG | 146845 |
| rs777581104 | snp | C/T | 1.65644e-05 | 0.00287783 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585733 | AATTCCTGGCCACTT[C/T]TGCACCTGATTATTA | 146845 |
| rs777592603 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9594089 | TCGTTTTTAAGTAAC[C/T]TGTTGTGTTTTTTTC | 146845 |
| rs777628646 | snp | A/G | | | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575258 | TGCAAAATGCCTTAT[A/G]AACAAGTGCACAATT | 146845 |
| rs777755088 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636616 | CCTCTACCCCTCCTA[C/T]GAGGCACTGCCTCTA | 146845 |
| rs777777947 | snp | C/T | 1.65258e-05 | 0.00287448 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600056 | AAGATTTCTTTTTCT[C/T]GCTTCTTCAGGTGGA | 146845 |
| rs777787640 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9613218 | GGTGGTGGGTATTAC[G/T]AGGGCTTCTGGATCT | 146845 |
| rs777791821 | in-del | -/T | 0.000218429 | 0.0104483 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586868 | TACTTATTTTCTTTA[-/T]TTTTTTTTAACTTTT | 146845 |
| rs777838546 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9629634 | CTCACTGCAACCTCT[A/G]CCTCCCGTGTTCAAG | 146845 |
| rs777855266 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9610915 | CCAGTATTTCTTTGT[C/T]GTCATCTGTGGGCTA | 146845 |
| rs777896422 | in-del | -/GAGA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636248 | AGAAAGAAAGAAAGA[-/GAGA]AAGAGAAAGAAAAAT | 146845 |
| rs777903786 | snp | A/C | | | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642223 | GATGCCCTTCCCACC[A/C]AAACAAATGAATTAA | 146845 |
| rs777906711 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9578194 | CACATGTGTATTGAA[C/G]AAACATTGATGTAAT | 146845 |
| rs777930342 | in-del | -/C | 0.000214184 | 0.0103463 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600204 | TAGAGACCATCGCCA[-/C]TGCCCTGCCATTTTT | 146845 |
| rs778015293 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9587435 | TTTTAGCTGTTTGAG[A/G]AATCACCACCCTGCT | 146845 |
| rs778069241 | snp | C/T | 1.66557e-05 | 0.00288575 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586007 | CTCATTGTCAATTTA[C/T]CTAGAGGTGCCTCCC | 146845 |
| rs778069959 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9640947 | CTGCACCCAGCTGGC[C/T]GTATCGCATTTTCTT | 146845 |
| rs778098479 | snp | C/G | 0.000677266 | 0.0183895 | missense | CFAP52 | GRCh38.p7 | 17:9594238 | TGCCATCTGTGGCAG[C/G]CCTGCAGCCGGCCTC | 146845 |
| rs778132345 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9588169 | TTAGAGTGCAGGCGT[A/G]TAATTCCACTGTTAA | 146845 |
| rs778141727 | snp | C/G | | | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9577382 | AGAAAAAGGGACTGG[C/G]CCGCTCCGCTGAAAT | 146845 |
| rs778149853 | snp | C/T | 1.64803e-05 | 0.00287052 | missense | CFAP52 | GRCh38.p7 | 17:9594293 | ATCTTCTCCAGGTGC[C/T]GGGATGAGATGTTTA | 146845 |
| rs778154457 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636034 | AAAAAGTTAGCTGGG[C/T]GTGGCGGCAGGTGCC | 146845 |
| rs778264244 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9640314 | ACATGTGCCGTGGTG[A/G]TTTGCTGTACGGATC | 146845 |
| rs778270536 | snp | A/C/G/T | 0.000460338 | 0.0151655 | utr-variant-5-prime, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576658 | GAAGACGCTGCAGCC[A/C/G/T]CTAGGGAGGAGAGCA | 146845 |
| rs778322038 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9591731 | CAAAAACTGAAAAAT[G/T]AGCCAGGCACGGTGG | 146845 |
| rs778337076 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9638459 | CTGTTTTGAAGAAAT[A/G]CAAGCACCACTTTGC | 146845 |
| rs778381409 | snp | C/G | 1.65619e-05 | 0.00287762 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9628702 | ATTTGCAACCTGTGC[C/G]AAGAAGGATATCAGG | 146845 |
| rs778463578 | snp | G/T | 1.65479e-05 | 0.0028764 | missense | CFAP52 | GRCh38.p7 | 17:9612479 | ATATTGTCTTTCCAT[G/T]GTGAGTAGAAGAGAA | 146845 |
| rs778496660 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9589975 | GGTGCTCTTCACAGT[A/G]CTTGTGTGTTTCCTT | 146845 |
| rs778513893 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9637146 | CTTGTTACAAATGTC[A/G]ATTTTGATTCATTAA | 146845 |
| rs778553088 | in-del | -/AT | 1.64787e-05 | 0.00287038 | frameshift-variant | CFAP52 | GRCh38.p7 | 17:9612415 | GTGTCAGCTTCACGG[-/AT]ATTTCAAAGAGACGC | 146845 |
| rs778593441 | in-del | -/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9598943 | CACTCAGAGCCCACA[-/G]CACATTCCTATGCCA | 146845 |
| rs778630119 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636560 | TTTTATTTTAGAATC[A/G]GATGCCATTCCTCCA | 146845 |
| rs778658732 | snp | C/T | 1.64754e-05 | 0.00287009 | missense | CFAP52 | GRCh38.p7 | 17:9600091 | GATGATAGCTTTTTC[C/T]ACCTTGGCACCACGA | 146845 |
| rs778697067 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9581472 | CAATTTGCCATACAG[C/T]GTATATGATATGAGC | 146845 |
| rs778783448 | snp | C/G | 1.64743e-05 | 0.00287 | missense | CFAP52 | GRCh38.p7 | 17:9600179 | CGAAGGACAAATTCA[C/G]TTTGGTGAGTAGAGA | 146845 |
| rs778787211 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9597677 | GCGTGGTGGCGGGCA[C/T]CTGTAGTCCCAGCTA | 146845 |
| rs778800997 | in-del | -/A/T | 0.00309707 | 0.0392294 | intron-variant | CFAP52 | GRCh38.p7 | 17:9594161 | TGTTTTCTCTTTGAC[-/A/T]TTTTTTTTTTTGGTC | 146845 |
| rs778927562 | snp | A/G | 1.64817e-05 | 0.00287064 | intron-variant, synonymous-codon | CFAP52 | GRCh38.p7 | 17:9585924 | CTTGGCCATCTCCAG[A/G]TCTGGAGAGTACATC | 146845 |
| rs778964641 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9609085 | ATGTGCTTTATGGCC[C/T]CTGCTACCCCCAGGA | 146845 |
| rs779051391 | snp | A/G | 1.72121e-05 | 0.00293356 | missense, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643025 | TTATCTTTTTCAGGT[A/G]GAAATGACCATCTGG | 146845 |
| rs779056604 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9596343 | TGAGCTCAGGCAATC[C/T]ACCTGCCTCGGCCTC | 146845 |
| rs779089512 | snp | C/T | | | missense | CFAP52 | GRCh38.p7 | 17:9608191 | GGACTGCTGGTCTTC[C/T]GTAAAAGCCCTGGCT | 146845 |
| rs779120459 | snp | A/C | 1.73637e-05 | 0.00294644 | intron-variant | CFAP52 | GRCh38.p7 | 17:9608255 | AGTGGGGCTGGGTAG[A/C]GACCCACTAAACGGA | 146845 |
| rs779126556 | in-del | -/CAGA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636236 | AGAAAGAAAGAAAGA[-/CAGA]AAGAAAGAAAGAAAG | 146845 |
| rs779144741 | in-del | -/AGAA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9597863 | GAAAGAGAGAGAGAA[-/AGAA]AGAAAGAAAGAAAGA | 146845 |
| rs779171436 | snp | A/G | 1.6504e-05 | 0.00287258 | missense | CFAP52 | GRCh38.p7 | 17:9586744 | GAGAGCTGCTTGCTC[A/G]GCTGTCCCTTCACAA | 146845 |
| rs779267076 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9612795 | CAGACAGTCCCTGAC[C/T]TATGATTTTTTTTAT | 146845 |
| rs779270573 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9585216 | AATACAGAATCTCAA[A/C]CCCTTCTCAGACCTG | 146845 |
| rs779323282 | snp | C/G | 1.72003e-05 | 0.00293255 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598193 | GATTATTAAATGGGT[C/G]TCCATTTGATTGTGG | 146845 |
| rs779373103 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9623538 | TTTCAAGAAATTAAG[A/G]GAAGAAAAAATTTAA | 146845 |
| rs779412931 | in-del | -/TGC | | | downstream-variant-500B, upstream-variant-2KB, intron-variant | CFAP52, USP43 | GRCh38.p7 | 17:9643772 | AGAGAGAAATATGCA[-/TGC]TTTCTCAAAGAAAAT | 146845 |
| rs779514308 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9582688 | GTCACCCAGGCTGGA[C/G]TGCAGTGGCACAATC | 146845 |
| rs779542198 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9633977 | TGAGCCACCGCGCCT[A/G]GCCCATCTTATCTTT | 146845 |
| rs779586425 | snp | C/G | 0.000116864 | 0.0076432 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | CFAP52, STX8 | GRCh38.p7 | 17:9576749 | GCTGGAACTTGACGC[C/G]GTGATCGGCTTCAAT | 146845 |
| rs779596470 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9600710 | GCTGGGACTACAGGC[A/G]CCCGCCACCACGCCC | 146845 |
| rs779652994 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9602205 | ATAGGTATACACGTG[C/G]CATGGTGGTTTGCTG | 146845 |
| rs779678804 | in-del | -/AG | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636202 | GAAAGAAAGAAAGAA[-/AG]AAAGAAAGAAAGAAA | 146845 |
| rs779689784 | snp | A/G | 6.60317e-05 | 0.00574556 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9594319 | GTTTATGACTGCTGG[A/G]AAGTATGTGTCTGCG | 146845 |
| rs779738811 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9603467 | ACCCGCCTCGGCCTC[C/T]CAAAGTGCTGGGATT | 146845 |
| rs779751452 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9635769 | AAGAACTGAATGTTA[A/G]AAGTTTCTGGGCAGA | 146845 |
| rs779797045 | snp | C/T | 1.6483e-05 | 0.00287076 | stop-gained, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641811 | GGCATGGATATCACA[C/T]AGGAAGGGGTGCACT | 146845 |
| rs779816732 | snp | G/T | 5.15159e-05 | 0.00507497 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598208 | GTCCATTTGATTGTG[G/T]TTTTTTGTTTTTTTT | 146845 |
| rs779869707 | snp | C/T | 3.34773e-05 | 0.00409115 | missense | CFAP52 | GRCh38.p7 | 17:9598284 | ATAGAAAAATCTGGC[C/T]AACTGAGTGCCAAAC | 146845 |
| rs779903938 | in-del | -/A | 3.29669e-05 | 0.00405984 | frameshift-variant | CFAP52 | GRCh38.p7 | 17:9628805 | TTCATGAGGGACGGC[-/A]AAAGCATCATTTCAG | 146845 |
| rs779917604 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9595676 | TTTTTTTAGGACAAT[C/G]TGCATTCTATGTCTG | 146845 |
| rs779966953 | snp | A/G | 9.8881e-05 | 0.0070307 | missense, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643116 | ACATCACACGCATCC[A/G]CATAAGTCCAGGAAA | 146845 |
| rs780075825 | in-del | -/GGGTAGTTGGGCTAG | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631615 | TGTCTGGGGCTTAGT[-/GGGTAGTTGGGCTAG]GGGTGCAGGGACAGC | 146845 |
| rs780104201 | snp | C/T | 0.000323671 | 0.0127173 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642999 | CTATTGCAGCAATGC[C/T]ATATACGTGTTTATC | 146845 |
| rs780107266 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9628469 | ATTTTTAGTAGAAAC[A/G]GGGTTTCACCATGTT | 146845 |
| rs780118752 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9586393 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 146845 |
| rs780209016 | snp | A/G | 1.64947e-05 | 0.00287177 | missense | CFAP52 | GRCh38.p7 | 17:9628727 | ATCAGGGTGTGGCAC[A/G]CATCATCCAACAGGG | 146845 |
| rs780210446 | snp | A/G | | | upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576311 | AGAAGTATCAATTAT[A/G]TATATTTTTTATAGC | 146845 |
| rs780263909 | snp | C/T | 1.681e-05 | 0.00289909 | missense, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643184 | TTGCGATGGAAGTAC[C/T]CATATACCTCCTGAA | 146845 |
| rs780315362 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9600596 | TTGAGAAAGAGTCTC[A/G]CTCTGTCGCCCAGGC | 146845 |
| rs780321614 | snp | C/T | 4.94743e-05 | 0.0049734 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9632967 | CAATGCTCACAGGAT[C/T]GGCGTCACCGCCATC | 146845 |
| rs780366652 | snp | A/G | 3.32276e-05 | 0.00407586 | intron-variant | CFAP52 | GRCh38.p7 | 17:9635581 | TGTGATGGGGAGGAT[A/G]CAGTGATACCTGCAA | 146845 |
| rs780399162 | in-del | -/AGC | 0.000839886 | 0.0204753 | intron-variant, cds-indel | CFAP52 | GRCh38.p7 | 17:9585890 | CTTCCTACAGGGTCA[-/AGC]TGGCAACAACGTCTC | 146845 |
| rs780440313 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9606881 | ATTCTGGTCCTTGCC[C/T]TCACATTCTTGAGCC | 146845 |
| rs780464216 | snp | A/G | 0.000112568 | 0.00750143 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584383 | CCTGGTGGGCACTCA[A/G]AACTGAAACCGAAAG | 146845 |
| rs780478188 | in-del | -/CA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9585671 | TGCAAGACTCTGTCA[-/CA]CACACACACACACAC | 146845 |
| rs780563499 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9581133 | CATCCTGGCTAACAC[A/G]GTGAAACCCCGTCTC | 146845 |
| rs780664297 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9593063 | CTTGGTTATACCTTG[A/G]TTTCAGACCAATGTG | 146845 |
| rs780675059 | snp | A/C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9582794 | GGTGTCCACCACTAC[A/C/G]CCCAGCTAATTTTTG | 146845 |
| rs780714617 | snp | A/G | 6.6011e-05 | 0.00574466 | missense | CFAP52 | GRCh38.p7 | 17:9586791 | CTGGCCTTTTCTCCA[A/G]ATGATTTGTACTTGG | 146845 |
| rs780725087 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631870 | CCTCCCGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 146845 |
| rs780743106 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9579757 | ATTTTTAATAGACAC[A/G]GTGTTTCGCCACGTT | 146845 |
| rs780833074 | snp | A/G | 1.67251e-05 | 0.00289176 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9598303 | TGAGTGCCAAACAGG[A/G]CAGTTGAAAAGAATA | 146845 |
| rs780871387 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9581293 | ATGCCACTGAATTGT[G/T]CACGTTAAAACAGTT | 146845 |
| rs780893740 | snp | A/G | 1.64803e-05 | 0.00287052 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9638660 | CTTATTCCAGTGTGT[A/G]TGCTATCACCCTGAG | 146845 |
| rs780939657 | snp | A/G | 4.94482e-05 | 0.00497209 | missense | CFAP52 | GRCh38.p7 | 17:9628802 | GACTTCATGAGGGAC[A/G]GCAAAAGCATCATTT | 146845 |
| rs780962898 | in-del | -/AGAAAGAAAGAAAGAAAGAG | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636234 | GAAAGAAAGAAAGAA[-/AGAAAGAAAGAAAGAAAGAG]AAAGAAAAATAACTA | 146845 |
| rs780998872 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9634287 | CCAACATAGGCACTA[C/T]AAGAAGGCGTAAGCA | 146845 |
| rs781024234 | in-del | -/AC | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9606387 | CTGTCTCCAAAATAC[-/AC]ACACACACACACACA | 146845 |
| rs781029748 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9586316 | TGCCTGTAATCCCAG[A/C]ACTTTGGGAGGCCTA | 146845 |
| rs781069013 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9607738 | GGATGTAAAAGTGTT[A/G]ATTTTTAAAATATTC | 146845 |
| rs781103649 | snp | A/G | 1.64925e-05 | 0.00287158 | missense | CFAP52 | GRCh38.p7 | 17:9632971 | GCTCACAGGATCGGC[A/G]TCACCGCCATCGCCA | 146845 |
| rs781127780 | snp | C/G | 2.23048e-05 | 0.00333944 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575789 | CCCTCACCCGGGACT[C/G]ACCAGGGGTCCGGTG | 146845 |
| rs781133526 | snp | C/G | | | upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576092 | GTGGGAGCGCTGCAA[C/G]ACCTCTCTGTAGCAG | 146845 |
| rs781145312 | snp | C/T | | | upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576308 | CAAAGAAGTATCAAT[C/T]ATATATATTTTTTAT | 146845 |
| rs781171629 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9626142 | CAGACCCTAAACTAA[A/G]AACAATCTACCACTT | 146845 |
| rs781265954 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9598979 | GCTATTTCTGCCACT[A/G]AAAATAAAGTTTCTG | 146845 |
| rs781268945 | in-del | -/TTT | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9611960 | CTGATTTTAGGATTA[-/TTT]TTCAGAAGTGGAATT | 146845 |
| rs781277228 | snp | G/T | 4.95123e-05 | 0.00497531 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598217 | ATTGTGGTTTTTTGT[G/T]TTTTTTTTTTACATA | 146845 |
| rs781327094 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9597930 | TGCTCTGCCCATGTT[C/T]CCTGCTTACTTGTGT | 146845 |
| rs781352856 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9585728 | TAGAAAATTCCTGGC[C/G]ACTTCTGCACCTGAT | 146845 |
| rs781359283 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9632687 | AGGAAGACTCAGGCT[A/G]TTGGCTTAGGCAACT | 146845 |
| rs781381423 | snp | C/G | 0.000231401 | 0.0107539 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575854 | TCCTGCTCTTAGCAG[C/G]TGACTACGGCGGCCC | 146845 |
| rs781388844 | in-del | -/CAA | 3.29516e-05 | 0.00405891 | intron-variant, cds-indel | CFAP52 | GRCh38.p7 | 17:9585894 | CCTACAGGGTCATGG[-/CAA]CAACGTCTCCTGCTT | 146845 |
| rs781430506 | snp | G/T | 6.94782e-05 | 0.00589358 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633069 | AAAAAATAACGCTCT[G/T]TTTAGAACAACTGCC | 146845 |
| rs781451495 | in-del | -/TGCTGTCCTACTA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9591939 | CTTATAAAGAAACTG[-/TGCTGTCCTACTA]TGCAAAAGGATCCAA | 146845 |
| rs781466856 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9613579 | CTGGAGTGCAGTGGT[A/G]GGATTTCGACTCACT | 146845 |
| rs781483659 | snp | C/G | 1.64765e-05 | 0.00287019 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600193 | AGTTTGGTGAGTAGA[C/G]ACCATCGCCACTGCC | 146845 |
| rs781501579 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9590669 | TCCCACCCCCTGTCA[A/C]AGAGACTAGGTCTTG | 146845 |
| rs781562210 | snp | C/G | 1.64923e-05 | 0.00287156 | missense | CFAP52 | GRCh38.p7 | 17:9594221 | AGCATAGCCAAGAGA[C/G]ATGCCATCTGTGGCA | 146845 |
| rs781632763 | snp | A/T | 1.64798e-05 | 0.00287047 | stop-gained | CFAP52 | GRCh38.p7 | 17:9612444 | GCTCATAGCGACTTG[A/T]CACTTTGATGCTGTC | 146845 |
| rs781683830 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9591633 | CTGTAATCCAAGCAC[C/T]TTGGGAGGCCAAGGC | 146845 |
| rs781696715 | snp | G/T | 1.65231e-05 | 0.00287424 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586882 | TATTTTTTTTAACTT[G/T]TATTTCAGGTTCAGA | 146845 |
| rs781726811 | snp | A/G | | | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642397 | GGGAGGCCAAGGCAG[A/G]TGGATCACCTGGGGT | 146845 |
| rs796112228 | in-del | -/AG | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636252 | AAGAAAGAAAGAAAG[-/AG]AAAGAAAAATAACTA | 146845 |
| rs796137607 | in-del | C/TTT | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9640239 | TTTTTTTTTTTTTTT[C/TTT]TCAACTTTAAGTTCA | 146845 |
| rs796206329 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9607328 | TCCAGTCTGAGTGAC[A/G]GAGAGAGACTCTGCC | 146845 |
| rs796227791 | in-del | -/TGTTTT | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9593447 | TAATTCTTTTGTTTG[-/TGTTTT]TGTTTTTGTTTTTGT | 146845 |
| rs796234636 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9585045 | TTTTATATTTACCCA[A/G]CCTTTGCCTGAGGTA | 146845 |
| rs796248697 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9585484 | CCAGCCTGACCAACA[C/T]GGTGAAACCCCGTCT | 146845 |
| rs796249018 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9616933 | TGGAAACTCTAAAAC[A/G]CAGAGCGCCTCTCCT | 146845 |
| rs796270471 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9632216 | CCGAGTAGCTAGGAC[A/T]AAATGGGCATGCCAC | 146845 |
| rs796314327 | in-del | -/TATGTATA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9596059 | ATATATATGTGTGTG[-/TATGTATA]TATATATATATATAT | 146845 |
| rs796331392 | in-del | -/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9591230 | TTAGTAGAGACGGGG[-/G]TCTCTTCATGTTGGT | 146845 |
| rs796349830 | in-del | -/TGAAA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9623338 | TCAAAGTACATCTCT[-/TGAAA]TGAAACAGCATATAC | 146845 |
| rs796404553 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9609983 | TAAAACCTGGAATCT[C/G]ATTTCTGGAGAGAGA | 146845 |
| rs796428248 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9637094 | AAACCCGACAAAGCA[A/C]GCTTTTGTCTTCTAG | 146845 |
| rs796454688 | in-del | -/TT | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9598216 | GATTGTGGTTTTTTG[-/TT]TTTTTTTTTTACATA | 146845 |
| rs796476299 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9607078 | TGGCTGAGTGTGGTG[A/G]CTCACACCTGTAATC | 146845 |
| rs796483160 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9588506 | TGTTGATGAGAGCTG[C/G]TGCTGAATAAAATCA | 146845 |
| rs796501679 | in-del | -/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9602396 | TTTCTGTTCCTGTTT[-/T]AGTTTGCTGAGAATG | 146845 |
| rs796502572 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9597851 | AGAAAGAGAGAGAGA[A/G]AGAGAGAGAGAAAGA | 146845 |
| rs796552041 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9607079 | GGCTGAGTGTGGTGG[C/G]TCACACCTGTAATCC | 146845 |
| rs796557137 | in-del | -/A | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9609249 | AAGATGAAAAAAAAA[-/A]TCCCTGTCCTCATGG | 146845 |
| rs796609825 | in-del | -/AGAAAGAAAG | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631021 | GAAAGAAAGAAAGAA[-/AGAAAGAAAG]AGAGAGAGAGAGAGA | 146845 |
| rs796743264 | in-del | -/A | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9580704 | AAAAAAAAAAAAAAA[-/A]TGCTGTTAAAGCAGT | 146845 |
| rs796762666 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9633665 | GTGGTTGTACGAATT[A/G]TCATCTTATCTTTTT | 146845 |
| rs796778857 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9584036 | ATAATGATCAAAGCA[A/T]TTTTGTGAAACATGT | 146845 |
| rs796803304 | in-del | -/A | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9637073 | AACAAACAAAAAAGC[-/A]AAAAAAAACCCGACA | 146845 |
| rs796831096 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9630961 | ACTGCACTCCAGCCT[C/G]GGTAACAGAGCCAGA | 146845 |
| rs796840502 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9625596 | TTAGCTGGTAACGCT[A/G]TGGTTTTTCTGCCAC | 146845 |
| rs796910382 | in-del | -/AA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9639431 | GCAAGACTCTCTCTT[-/AA]AAAAAAAAAAAAATT | 146845 |
| rs796927379 | in-del | AAA/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9589749 | AAAAAAAAAAAAAAA[AAA/T]AAGAAAAGAAATGTA | 146845 |
| rs796931145 | in-del | -/AGAGAGAGAGAGAGAGAGAGAGAG | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631029 | GAAAGAAAGAAAGAA[-/AGAGAGAGAGAGAGAGAGAGAGAG]AGAAAGAAAGAAAGA | 146845 |
| rs797013726 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9632255 | GCAAGTTTTTTTTTG[G/T]TTTTTTTTTTCATAT | 146845 |